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Omeprazole - Medication Information

Product NDC Code 11822-0061
Drug Name

Omeprazole

Type Generic
Pharm Class Cytochrome P450 2C19 Inhibitors [MoA],
Proton Pump Inhibitor [EPC],
Proton Pump Inhibitors [MoA]
Active Ingredients
Omeprazole magnesium 20.6 mg/1
Route ORAL
Dosage Form CAPSULE, DELAYED RELEASE
RxCUI drug identifier 198051
Application Number ANDA210593
Labeler Name Rite Aid
Packages
Package NDC Code Description
11822-0061-4 3 bottle in 1 carton (11822-0061-4) / 14 capsule, delayed release in 1 bottle (11822-0061-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each capsule) *Omeprazole delayed-release capsule 20 mg (equivalent to 20.6 mg omeprazole magnesium, USP)

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions ▪ for adults 18 years of age and older ■ this product is to be used once a day (every 24 hours), every day for 14 days ■ it may take 1 to 4 days for full effect; some people get complete relief of symptoms within 24 hours 14-Day Course of Treatment ■ swallow 1 capsule with a glass of water before eating in the morning ■ take every day for 14 days ■ do not take more than 1 capsule a day ■ do not use for more than 14 days unless directed by your doctor ■ swallow whole. Do not chew or crush capsules. Repeated 14-Day Courses (if needed) ■ you may repeat a 14-day course every 4 months ■ do not take for more than 14 days or more often than every 4 months unless directed by a doctor ■ children under 18 years of age: ask a doctor. Heartburn in children may sometimes be caused by a serious condition. Other Safety Information ■ read the directions and warnings before use ■ keep the carton. It contains important information. ■ Store at 20-25°C (68-77°F). [See USP controlled room temperature]. Protect from moisture

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients FD&C blue #1, FD&C red #40, ferrosoferric oxide, gelatin, hydroxypropyl cellulose, hypromellose, magnesium carbonate, magnesium stearate, methacrylic acid copolymer, mono and diglycerides, polyethylene glycol 6000, polysorbate 80, potassium hydroxide, propylene glycol, shellac, sodium stearyl fumarate, sugar spheres (starch and sucrose), talc, titanium dioxide and triethyl citrate Questions? Call toll-free Monday to Friday 8:30 am to 5 pm EST at 1800-406-7984

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use ▪ treats frequent heartburn (occurs 2 or more days a week) ▪ not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

Purpose

Information about the drug product’s indications for use.
Purpose Acid reducer

Spl product data elements

Usually a list of ingredients in a drug product.
omeprazole omeprazole OMEPRAZOLE MAGNESIUM OMEPRAZOLE FERROSOFERRIC OXIDE GELATIN, UNSPECIFIED HYDROXYPROPYL CELLULOSE, UNSPECIFIED HYPROMELLOSE 2208 (100 MPA.S) MAGNESIUM CARBONATE MAGNESIUM STEARATE METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER POLYSORBATE 80 POTASSIUM HYDROXIDE PROPYLENE GLYCOL SHELLAC SODIUM STEARYL FUMARATE TALC TITANIUM DIOXIDE TRIETHYL CITRATE STARCH, CORN SUCROSE FD&C BLUE NO. 1 FD&C RED NO. 40 POLYETHYLENE GLYCOL 6000 RG49

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL - 42 Capsule Bottle Carton NDC 11822-0061-4 TREATS FREQUENT HEARTBURN Compare to the active ingredient of Prilosec OTC ®† OMEPRAZOLE Delayed-release Capsules 20 mg* ACID REDUCER Mini Cap 40% Smaller Capsule 24 HR ACTUAL SIZE 42 CAPSULES THREE 14-DAY COURSES OF TREATMENT MAY TAKE 1 TO 4 DAYS FOR FULL EFFECT TRIPLE PACK 3 X 14 COUNT BOTTLE INSIDE Principal Display Panel - 42 Capsule Bottle Carton

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep Out of Reach of Children

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Safety Information ■ read the directions and warnings before use ■ keep the carton. It contains important information. ■ Store at 20-25°C (68-77°F). [See USP controlled room temperature]. Protect from moisture

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Call toll-free Monday to Friday 8:30 am to 5 pm EST at 1800-406-7984

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Allergy alert: Do not use if you are allergic to omeprazole Do not use if you have: ■ trouble or pain swallowing food, vomiting with blood, or bloody or black stools ■ heartburn with lightheadedness, sweating or dizziness ■ chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness ■ frequent chest pain These may be signs of a serious condition. See your doctor Ask a doctor before use if you have: ■ had heartburn over 3 months. This may be a sign of a more serious condition. ■ frequent wheezing, particularly with heartburn ■ unexplained weight loss ■ nausea or vomiting ■ stomach pain Ask a doctor or pharmacist before use if you are taking a prescription drug. Acid reducers may interact with certain prescription drugs. Stop use and ask a doctor if: ■ your heartburn continues or worsens ■ you need to take this product for more than 14 days ■ you need to take more than 1 course of treatment every 4 months ■ you get diarrhea ■ you develop a rash or joint pain If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API