Loproc Uses

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What is Loproc?

Loproc + SyrSpend SF Alka is a proton pump inhibitor that decreases the amount of acid produced in the stomach.

Loproc + SyrSpend SF Alka is used to treat symptoms of gastroesophageal reflux disease (GERD) and other conditions caused by excess stomach acid. Loproc + SyrSpend SF Alka is also used to promote healing of erosive esophagitis (damage to your esophagus caused by stomach acid).

Loproc + SyrSpend SF Alka may also be given together with antibiotics to treat gastric ulcer caused by infection with Helicobacter pylori (H. pylori).

Over-the-counter (OTC) Loproc + SyrSpend SF Alka is used to help control heartburn that occurs 2 or more days per week. Loproc + SyrSpend SF Alka + SyrSpend SF Alka not for immediate relief of heartburn symptoms. OTC Loproc + SyrSpend SF Alka must be taken on a regular basis for 14 days in a row.

Loproc + SyrSpend SF Alka may also be used for purposes not listed in this medication guide.

Loproc indications

infoAn indication is a term used for the list of condition or symptom or illness for which the medicine is prescribed or used by the patient. For example, acetaminophen or paracetamol is used for fever by the patient, or the doctor prescribes it for a headache or body pains. Now fever, headache and body pains are the indications of paracetamol. A patient should be aware of the indications of medications used for common conditions because they can be taken over the counter in the pharmacy meaning without prescription by the Physician.
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Duodenal Ulcer (adults)

Loproc is indicated for short-term treatment of active duodenal ulcer in adults. Most patients heal within four weeks. Some patients may require an additional four weeks of therapy.

Loproc in combination with clarithromycin and amoxicillin, is indicated for treatment of patients with H. pylori infection and duodenal ulcer disease (active or up to 1-year history) to eradicate H. pylori in adults.

Loproc in combination with clarithromycin is indicated for treatment of patients with H. pylori infection and duodenal ulcer disease to eradicate H. pylori in adults.

Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.

Among patients who fail therapy, Loproc with clarithromycin is more likely to be associated with the development of clarithromycin resistance as compared with triple therapy. In patients who fail therapy, susceptibility testing should be done. If resistance to clarithromycin is demonstrated or susceptibility testing is not possible, alternative antimicrobial therapy should be instituted, and the clarithromycin package insert, Microbiology section.

Gastric Ulcer (Adults)

Loproc is indicated for short-term treatment (4-8 weeks) of active benign gastric ulcer in adults.

Treatment Of Gastroesophageal Reflux Disease (GERD) (Adults and Pediatric Patients)

Symptomatic GERD

Loproc is indicated for the treatment of heartburn and other symptoms associated with GERD in pediatric patients and adults for up to 4 weeks.

Erosive Esophagitis

Loproc is indicated for the short-term treatment (4-8 weeks) of erosive esophagitis that has been diagnosed by endoscopy in pediatric patients and adults.

The efficacy of Loproc used for longer than 8 weeks in these patients has not been established. If a patient does not respond to 8 weeks of treatment, an additional 4 weeks of treatment may be given. If there is recurrence of erosive esophagitis or GERD symptoms (eg, heartburn), additional 4-8 week courses of Loproc may be considered.

Maintenance Of Healing Of Erosive Esophagitis (Adults and Pediatric Patients)

Loproc is indicated to maintain healing of erosive esophagitis in pediatric patients and adults.

Controlled studies do not extend beyond 12 months.

Pathological Hypersecretory Conditions (Adults)

Loproc is indicated for the long-term treatment of pathological hypersecretory conditions (eg, Zollinger-Ellison syndrome, multiple endocrine adenomas and systemic mastocytosis) in adults.

How should I use Loproc?

Use Loproc delayed-release oral suspension as directed by your doctor. Check the label on the medicine for exact dosing instructions.

  • Loproc delayed-release oral suspension comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Loproc delayed-release oral suspension refilled.
  • Take Loproc delayed-release oral suspension by mouth before a meal or as directed by your doctor.
  • Mix Loproc delayed-release oral suspension in a small amount of water before taking your dose. Use an oral syringe to measure the amount of water needed to mix your dose. Ask your pharmacist for an oral syringe. The recommended amount of water for mixing each dose is as follows:
    • If your dose of Loproc delayed-release oral suspension is 2.5 mg, add 1 teaspoon (5 mL) of water to a container.
    • If your dose of Loproc delayed-release oral suspension is 10 mg, add 1 tablespoon (15 mL) of water to a container.
  • Tear open the medicine packet and add the contents of the packet to the container. Stir well. Allow the mixture to thicken for 2 to 3 minutes. Stir again. Drink the mixture within 30 minutes. If it is not used within 30 minutes, throw it away and mix a new dose. If any medicine remains in the glass after drinking, add more water. Stir, then drink right away.
  • If your doctor has instructed you to use more than 1 packet for your dose, follow the mixing instructions provided by your doctor or pharmacist.
  • If the patient is taking Loproc delayed-release oral suspension through a nasogastric (NG) tube or gastric tube, follow the instructions for use in the extra patient leaflet.
  • You may take antacids while you are using Loproc delayed-release oral suspension if you are directed to do so by your doctor.
  • Continue to take Loproc delayed-release oral suspension even if you feel well. Do not miss any doses.
  • If you miss a dose of Loproc delayed-release oral suspension, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Loproc delayed-release oral suspension.

Uses of Loproc in details

infoThere are specific as well as general uses of a drug or medicine. A medicine can be used to prevent a disease, treat a disease over a period or cure a disease. It can also be used to treat the particular symptom of the disease. The drug use depends on the form the patient takes it. It may be more useful in injection form or sometimes in tablet form. The drug can be used for a single troubling symptom or a life-threatening condition. While some medications can be stopped after few days, some drugs need to be continued for prolonged period to get the benefit from it.
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Loproc is used to treat frequent persistent heartburn, gastro-esophageal reflux disease (GERD; flow of bitter fluid into mouth, and upper abdominal/ epigastric pain); and other diseases caused by excessive stomach acid. It is also used to help in the healing of the food pipe (esophagus) when it gets damaged by excessive stomach acid ( erosive esophagitis).

Loproc description

The active ingredient in Loproc is a substituted benzimidazole. (RS)-5-methoxy-2(4-methoxy-3,5-dimethyl-2-pyridylmethylsulphinyl) benzimidazole, a compound that inhibits gastric acid secretion. Its empirical formula is C17H19N3O3S, with a molecular weight of 345.42. Loproc is a white to off-white crystalline powder which melts with decomposition at about 155°C. It is a weak base, freely soluble in ethanol and methanol, and slightly soluble in acetone and isopropanol and very slightly soluble in water. The stability of Loproc is a function of pH; it is rapidly degraded in acid media, but has acceptable stability under alkaline conditions.

Loproc is a proton pump inhibitor. It inhibits secretion of gastric acid by irreversibly blocking the enzyme system of hydrogen/potassium adenosine triphosphatase (H+/K+ ATPase), the "proton pump" of the gastric parietal cell. It is used in conditions where inhibition of gastric acid secretion may be beneficial, including aspiration syndromes, dyspepsia, gastro-esophageal reflux disease, peptic ulcer disease and the Zollinger-Ellison syndrome.

Loproc dosage

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Loproc Delayed-Release Capsules should be taken before eating. In the clinical trials, antacids were used concomitantly with Loproc.

Patients should be informed that the Loproc Delayed-Release Capsule should be swallowed whole.

For patients unable to swallow an intact capsule, alternative administration options are available.

Short-Term Treatment Of Active Duodenal Ulcer

The recommended adult oral dose of Loproc is 20 mg once daily. Most patients heal within four weeks. Some patients may require an additional four weeks of therapy.

H. pylori Eradication For The Reduction Of The Risk Of Duodenal Ulcer Recurrence

Triple Therapy (Loproc/clarithromycin/amoxicillin)

The recommended adult oral regimen is Loproc 20 mg plus clarithromycin 500 mg plus amoxicillin 1000 mg each given twice daily for 10 days. In patients with an ulcer present at the time of initiation of therapy, an additional 18 days of Loproc 20 mg once daily is recommended for ulcer healing and symptom relief.

Dual Therapy (Loproc/clarithromycin)

The recommended adult oral regimen is Loproc 40 mg once daily plus clarithromycin 500 mg three times daily for 14 days. In patients with an ulcer present at the time of initiation of therapy, an additional 14 days of Loproc 20 mg once daily is recommended for ulcer healing and symptom relief.

Gastric Ulcer

The recommended adult oral dose is 40 mg once daily for 4-8 weeks.

Gastroesophageal Reflux Disease (GERD)

The recommended adult oral dose for the treatment of patients with symptomatic GERD and no esophageal lesions is 20 mg daily for up to 4 weeks. The recommended adult oral dose for the treatment of patients with erosive esophagitis and accompanying symptoms due to GERD is 20 mg daily for 4 to 8 weeks.

Maintenance Of Healing Of Erosive Esophagitis

The recommended adult oral dose is 20 mg daily. Controlled studies do not extend beyond 12 months.

Pathological Hypersecretory Conditions

The dosage of Loproc in patients with pathological hypersecretory conditions varies with the individual patient. The recommended adult oral starting dose is 60 mg once daily. Doses should be adjusted to individual patient needs and should continue for as long as clinically indicated. Doses up to 120 mg three times daily have been administered. Daily dosages of greater than 80 mg should be administered in divided doses. Some patients with Zollinger-Ellison syndrome have been treated continuously with Loproc for more than 5 years.

Pediatric Patients

For the treatment of GERD and maintenance of healing of erosive esophagitis, the recommended daily dose for pediatric patients 1 to 16 years of age is as follows:

Patient Weight Loproc Daily Dose
5 < 10 kg 5 mg
10 < 20 kg 10 mg
≥ 20 kg 20 mg

On a per kg basis, the doses of Loproc required to heal erosive esophagitis in pediatric patients are greater than those for adults.

Alternative administrative options can be used for pediatric patients unable to swallow an intact capsule.

Alternative Administration Options

Loproc is available as a delayed-release capsule or as a delayed-release oral suspension.

For patients who have difficulty swallowing capsules, the contents of a Loproc Delayed-Release Capsule can be added to applesauce.

One tablespoon of applesauce should be added to an empty bowl and the capsule should be opened. All of the pellets inside the capsule should be carefully emptied on the applesauce. The pellets should be mixed with the applesauce and then swallowed immediately with a glass of cool water to ensure complete swallowing of the pellets. The applesauce used should not be hot and should be soft enough to be swallowed without chewing. The pellets should not be chewed or crushed. The pellets/applesauce mixture should not be stored for future use.

Loproc For Delayed-Release

Oral Suspension should be administered as follows:

  • Empty the contents of a 2.5 mg packet into a container containing 5 mL of water.
  • Empty the contents of a 10 mg packet into a container containing 15 mL of water.
  • Stir
  • Leave 2 to 3 minutes to thicken.
  • Stir and drink within 30 minutes.
  • If any material remains after drinking, add more water, stir and drink immediately.

For patients with a nasogastric or gastric tube in place:

  • Add 5 mL of water to a catheter tipped syringe and then add the contents of a 2.5 mg packet (or 15 mL of water for the 10 mg packet). It is important to only use a catheter tipped syringe when administering Loproc through a nasogastric tube or gastric tube.
  • Immediately shake the syringe and leave 2 to 3 minutes to thicken.
  • Shake the syringe and inject through the nasogastric or gastric tube, French size 6 or larger, into the stomach within 30 minutes.
  • Refill the syringe with an equal amount of water.
  • Shake and flush any remaining contents from the nasogastric or gastric tube into the stomach.

How supplied

Dosage Forms And Strengths

Loproc Delayed-Release Capsules, 10 mg, are opaque, hard gelatin, apricot and amethyst colored capsules, coded 606 on cap and Loproc 10 on the body.

Loproc Delayed-Release Capsules, 20 mg, are opaque, hard gelatin, amethyst colored capsules, coded 742 on cap and Loproc 20 on the body.

Loproc Delayed-Release Capsules, 40 mg, are opaque, hard gelatin, apricot and amethyst colored capsules, coded 743 on cap and Loproc 40 on the body.

Loproc For Delayed-Release

Oral Suspension, 2.5 mg or 10 mg, is supplied as a unit dose packet containing a fine yellow powder, consisting of white to brownish Loproc granules and pale yellow inactive granules.

Storage And Handling

Loproc Delayed-Release Capsules, 10 mg, are opaque, hard gelatin, apricot and amethyst colored capsules, coded 606 on cap and Loproc 10 on the body. They are supplied as follows:

NDC 0186-0606-31 unit of use bottles of 30

Loproc Delayed-Release Capsules, 20 mg, are opaque, hard gelatin, amethyst colored capsules, coded 742 on cap and Loproc 20 on body. They are supplied as follows:

NDC 0186-0742-31 unit of use bottles of 30

NDC 0186-0742-82 bottles of 1000

Loproc Delayed-Release Capsules, 40 mg, are opaque, hard gelatin, apricot and amethyst colored capsules, coded 743 on cap and Loproc 40 on the body. They are supplied as follows:

NDC 0186-0743-31 unit of use bottles of 30

NDC 0186-0743-68 bottles of 100

Loproc For Delayed-Release

Oral Suspension, 2.5 mg or 10 mg

, is supplied as a unit dose packet containing a fine yellow powder, consisting of white to brownish Loproc granules and pale yellow inactive granules. Loproc unit dose packets are supplied as follows:

NDC 0186-0625-01 unit dose packages of 30: 2.5 mg packets

NDC 0186-0610-01 unit dose packages of 30: 10 mg packets

Storage

Store Loproc Delayed-Release Capsules in a tight container protected from light and moisture. Store between 15°C and 30°C (59°F and 86°F).

Store Loproc For Delayed-Release

Oral Suspension at 25°C (77°F); excursions permitted to 15 – 30°C (59 – 86°F).

AstraZeneca Pharmaceuticals LP Wilmington, DE 19850. Revised December 2014

Loproc interactions

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What other drugs will affect Loproc?

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Effects of Loproc on the Pharmacokinetics of Other Drugs: The following combination with Loproc should be avoided: Ketoconazole and itraconazole.

Loproc might influence the absorption of other drugs due to its effect on the gastric pH. The dissolution of ketoconazole tablets in the stomach is adversely affected if the pH of the gastric juice increases as a result of drug treatment (antacids, secretion-inhibiting agents, sucralfate). This leads to ineffective plasma concentrations of ketoconazole. During concomitant administration of Loproc and itraconazole, the plasma concentration and area under the curve (AUC) of itraconazole are reduced by approximately 65%, probably as a result of poorer absorption, which is dependent on pH.

Loproc inhibits the enzyme CYP2C19 and therefore, increased plasma levels of other drugs (diazepam, warfarin, phenytoin) metabolized via this enzyme might be expected. Monitoring is recommended during initiation or withdrawal of Loproc in patients being treated with phenytoin, warfarin or other vitamin K antagonist.

During concomitant administration of clarithromycin or erythromycin and Loproc, the plasma concentrations of Loproc were increased. The plasma concentrations of Loproc are not influenced during concomitant administration with amoxicillin or metronidazole.

Concomitant administration of Loproc (40 mg once daily) and atazanavir 300 mg/ritonavir 100 mg to healthy volunteers resulted in a marked reduction in total atazanavir exposure (approximately 75% reduction of AUC, Cmax and Cmin). An increase in the atazanavir dose to 400 mg did not compensate for the effect that Loproc had on atazanavir exposure. Proton pump inhibitors including Loproc should therefore not be administered concomitantly with atazanavir.

Concomitant administration of Loproc and tacrolimus may increase the serum levels of tacrolimus. Monitoring of the plasma tacrolimus concentration is recommended when treatment with Loproc is being initiated or discontinued. Loproc (40 mg daily) increased the Cmax and AUC of voriconazole (CYP2C19 substrate) by 15% and 41%, respectively.

Effects of Other Drugs on the Pharmacokinetics of Loproc: Drugs inhibiting the enzymes CYP2C19 or CYP3A (HIV protease inhibitors, ketoconazole, itraconazole) might increase the plasma concentrations of Loproc. Voriconazole increases the AUC of Loproc by 280%. In cases of concomitant treatment, an adjustment of the Loproc dose should be considered for patients with considerable impaired hepatic function and in cases of long-term treatment.

Case reports, published population pharmacokinetic studies and retrospective analyses suggest that concomitant administration of PPIs and methotrexate (primarily at high doses) may elevate and prolong serum levels of methotrexate and/or its metabolite hydroxymethotrexate. However, no formal drug interaction studies of methotrexate with PPIs have been conducted.

No interactions between Loproc and antacids, theophylline, caffeine, quinidine, lidocaine, propranolol, metoprolol or ethanol have been detected.

Loproc side effects

See also:
What are the possible side effects of Loproc?

Clinical Trials Experience With Loproc Monotherapy

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

The safety data described below reflects exposure to Loproc Delayed-Release Capsules in 3096 patients from worldwide clinical trials (465 patients from US studies and 2,631 patients from international studies). Indications clinically studied in US trials included duodenal ulcer, resistant ulcer, and Zollinger-Ellison syndrome. The international clinical trials were double blind and open-label in design. The most common adverse reactions reported (i.e., with an incidence rate ≥ 2%) from Loproc-treated patients enrolled in these studies included headache (6.9%), abdominal pain (5.2%), nausea (4.0%), diarrhea (3.7%), vomiting (3.2%), and flatulence (2.7%).

Additional adverse reactions that were reported with an incidence ≥ 1% included acid regurgitation (1.9%), upper respiratory infection (1.9%), constipation (1.5%), dizziness (1.5%), rash (1.5%), asthenia (1.3%), back pain (1.1%), and cough (1.1%).

The clinical trial safety profile in patients greater than 65 years of age was similar to that in patients 65 years of age or less.

The clinical trial safety profile in pediatric patients who received Loproc Delayed-Release Capsules was similar to that in adult patients. Unique to the pediatric population, however, adverse reactions of the respiratory system were most frequently reported in both the 1 to < 2 and 2 to 16 year age groups (75.0% and 18.5%, respectively). Similarly, fever was frequently reported in the 1 to 2 year age group (33.0%), and accidental injuries were reported frequently in the 2 to 16 year age group (3.8%).

Clinical Trials Experience With Loproc In Combination Therapy For H. pylori Eradication

In clinical trials using either dual therapy with Loproc and clarithromycin, or triple therapy with Loproc, clarithromycin, and amoxicillin, no adverse reactions unique to these drug combinations were observed. Adverse reactions observed were limited to those previously reported with Loproc, clarithromycin, or amoxicillin alone.

Dual Therapy (Loproc/clarithromycin)

Adverse reactions observed in controlled clinical trials using combination therapy with Loproc and clarithromycin (n = 346) that differed from those previously described for Loproc alone were taste perversion (15%), tongue discoloration (2%), rhinitis (2%), pharyngitis (1%) and flu-syndrome (1%). (For more information on clarithromycin, refer to the clarithromycin prescribing information, Adverse Reactions section.)

Triple Therapy (Loproc/clarithromycin/amoxicillin)

The most frequent adverse reactions observed in clinical trials using combination therapy with Loproc, clarithromycin, and amoxicillin (n = 274) were diarrhea (14%), taste perversion (10%), and headache (7%). None of these occurred at a higher frequency than that reported by patients taking antimicrobial agents alone. (For more information on clarithromycin or amoxicillin, refer to the respective prescribing information, Adverse Reactions sections.)

Post-marketing Experience

The following adverse reactions have been identified during post-approval use of Loproc Delayed-Release Capsules. Because these reactions are voluntarily reported from a population of uncertain size, it is not always possible to reliably estimate their actual frequency or establish a causal relationship to drug exposure.

Body As a Whole: Hypersensitivity reactions including anaphylaxis, anaphylactic shock, angioedema, bronchospasm, interstitial nephritis, urticaria,; fever; pain; fatigue; malaise;

Cardiovascular: Chest pain or angina, tachycardia, bradycardia, palpitations, elevated blood pressure, peripheral edema

Endocrine: Gynecomastia

Gastrointestinal: Pancreatitis (some fatal), anorexia, irritable colon, fecal discoloration, esophageal candidiasis, mucosal atrophy of the tongue, stomatitis, abdominal swelling, dry mouth, microscopic colitis. During treatment with Loproc, gastric fundic gland polyps have been noted rarely. These polyps are benign and appear to be reversible when treatment is discontinued.

Gastroduodenal carcinoids have been reported in patients with ZE syndrome on long-term treatment with Loproc. This finding is believed to be a manifestation of the underlying condition, which is known to be associated with such tumors.

Hepatic: Liver disease including hepatic failure (some fatal), liver necrosis (some fatal), hepatic encephalopathy hepatocellular disease, cholestatic disease, mixed hepatitis, jaundice, and elevations of liver function tests [ALT, AST, GGT, alkaline phosphatase, and bilirubin]

Infections and Infestations: Clostridium difficile associated diarrhea

Metabolism and Nutritional disorders: Hypoglycemia, hypomagnesemia, with or without hypocalcemia and/or hypokalemia, hyponatremia, weight gain

Musculoskeletal: Muscle weakness, myalgia, muscle cramps, joint pain, leg pain, bone fracture

Nervous System/Psychiatric: Psychiatric and sleep disturbances including depression, agitation, aggression, hallucinations, confusion, insomnia, nervousness, apathy, somnolence, anxiety, and dream abnormalities; tremors, paresthesia; vertigo

Respiratory: Epistaxis, pharyngeal pain

Skin: Severe generalized skin reactions including toxic epidermal necrolysis (some fatal), Stevens-Johnson syndrome, and erythema multiforme; photosensitivity; urticaria; rash; skin inflammation; pruritus; petechiae; purpura; alopecia; dry skin; hyperhidrosis

Special Senses: Tinnitus, taste perversion

Ocular: Optic atrophy, anterior ischemic optic neuropathy, optic neuritis, dry eye syndrome, ocular irritation, blurred vision, double vision

Urogenital: Interstitial nephritis, hematuria, proteinuria, elevated serum creatinine, microscopic pyuria, urinary tract infection, glycosuria, urinary frequency, testicular pain

Hematologic: Agranulocytosis (some fatal), hemolytic anemia, pancytopenia, neutropenia, anemia, thrombocytopenia, leukopenia, leucocytosis

Loproc contraindications

See also:
What is the most important information I should know about Loproc?

You should not take this medication if you are allergic to Loproc or to any other benzimidazole medication such as albendazole or mebendazole. Loproc is not for immediate relief of heartburn symptoms.

Ask a doctor or pharmacist if it is safe for you to take Loproc if you have liver disease or heart disease, or low levels of magnesium in your blood.

Some conditions are treated with a combination of Loproc and antibiotics. Use all medications as directed by your doctor. Read the medication guide or patient instructions provided with each medication. Do not change your doses or medication schedule without your doctor's advice.

Take this medication for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared.

Loproc OTC (over-the-counter) should be taken for no longer than 14 days in a row. Allow at least 4 months to pass before you start another 14-day treatment.

Heartburn is often confused with the first symptoms of a heart attack. Seek emergency medical attention if you have chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, and a general ill feeling.



Active ingredient matches for Loproc:

Omeprazole in Greece.


List of Loproc substitutes (brand and generic names)

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Unit description / dosage (Manufacturer)Price, USD
LORESS Capsule/ Tablet / 20mg / 10 units (Bio E)$ 0.62
LORESS Capsule/ Tablet / 10mg / 10 units (Bio E)$ 0.31
10 mg x 10's (Bio E)$ 0.31
20 mg x 10's (Bio E)$ 0.62
Loress 20mg CAP / 10 (Bio E)$ 0.62
Loress 10mg CAP / 10 (Bio E)$ 0.31
LORESS 10MG CAPSULE 1 strip / 10 capsules each (Bio E)$ 0.32
LORESS 20MG CAPSULE 1 strip / 10 capsules each (Bio E)$ 0.62
LORESS cap 10 mg x 10's (Bio E)$ 0.31
LORESS cap 20 mg x 10's (Bio E)$ 0.62
Loress 10mg CAP / 10 (Bio E)$ 0.31
Loress 20mg CAP / 10 (Bio E)$ 0.62
Loress 10mg Capsule (Bio E)$ 0.03
Loress 20mg Capsule (Bio E)$ 0.06
Losec 10 mg tablet / delayed-release 10 mg (Astrazeneca Canada Inc (Canada))
Losec 20 mg tablet / delayed-release 20 mg (Astrazeneca Canada Inc (Canada))
Tablet, Delayed Release; Oral; Omeprazole Magnesium 20 mg
Tablets, Delayed Release; Oral; Omeprazole Magnesium 20 mg
Injectable; Subcutaneous; Omeprazole 40 mg
Injectable; Injection; Omeprazole 40 mg
Injectable; Subcutaneous; Omeprazole 40 mg
Injectable; Injection; Omeprazole 40 mg
Injectable; Subcutaneous; Omeprazole 40 mg
Injectable; Injection; Omeprazole 40 mg
Tablet, Delayed Release; Oral; Omeprazole Magnesium 10 mg (AstraZeneca)
Tablet, Delayed Release; Oral; Omeprazole Magnesium 20 mg (AstraZeneca)
Tablet, Delayed Release; Oral; Omeprazole Magnesium 40 mg (AstraZeneca)
Losec MUPS 10 mg x 14's (AstraZeneca)$ 320.00
Losec MUPS 20 mg x 14's (AstraZeneca)$ 562.00
Tablets, Delayed Release; Oral; Omeprazole Magnesium 10 mg (AstraZeneca)

References

  1. DailyMed. "OMEPRAZOLE MAGNESIUM: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. PubChem. "omeprazole". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
  3. DrugBank. "omeprazole". http://www.drugbank.ca/drugs/DB00338 (accessed September 17, 2018).

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