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Acid Reducer

NDC 37835-189 · Bi-Mart

Generic nameOmeprazole
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)OMEPRAZOLE MAGNESIUM
Strength20 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

37835-189-14 — 1 BOTTLE in 1 CARTON (37835-189-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

37835-189-42 — 3 BOTTLE in 1 CARTON (37835-189-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21130-528 — Omeprazole magnesium, 21130-783 — Omeprazole, 25000-091 — Omeprazole 20 mg, 25000-094 — Omeprazole 20 mg, 30142-012 — Omeprazole Magnesium 20.6mg Capsules, 30142-077 — Omeprazole, 37000-455 — omeprazole magnesium, 37000-459 — OMEPRAZOLE MAGNESIUM, 37808-006 — Omeprazole Magnesium, 37808-569 — Omeprazole, 43598-813 — Omeprazole Magnesium, 46122-686 — OMEPRAZOLE, 49035-397 — Omeprazole Magnesium 20.6mg Capsules, 49035-983 — Omeprazole, 49483-731 — Omeprazole 20mg, 51316-061 — Omeprazole, 51316-271 — Omeprazole magnesium, 51316-843 — Omeprazole, 53943-016 — Omeprazole, 53943-520 — Omeprazole Magnesium, +56 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.