Active Ingredient(S)
Omeprazole USP, 20 mg
The following Structured Product Label (SPL) was submitted to the FDA by Bluepoint Laboratories for the product Omeprazole (NDC 68001-441). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use(s), warnings, do not use if you have:, ask a doctor before use if you have:, ask a doctor or pharmacist before use if you are, stop use and ask doctor if:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Omeprazole USP, 20 mg
Acid reducer
Allergy alert: Do not use if you are allergic to omeprazole
These may be signs of a serious condition. See your doctor.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)
14-Day Course of Treatment
Repeated 14-Day Courses (if needed)
ammonia solution, ammonium hydroxide, carnauba wax, hypromellose acetate succinate, hypromellose, iron oxide black, lactose monohydrate, monoethanolamine, n-butyl alcohol, polyethylene glycol, polyvinyl alcohol, povidone, propylene glycol, red iron oxide, sodium stearate, sodium starch glycolate, shellac glaze, sodium lauryl sulphate, sodium stearyl fumarate, talc, titanium dioxide, triethyl citrate, yellow iron oxide
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Distributed by:
Dr. Reddy’s Laboratories Inc.,
Princeton, NJ 08540
For BluePoint Laboratories
Made in India
Revised:05/20
Container carton: 14's pack
Bottle Label: 14's pack
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