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Omeprazole

NDC 63941-997 · VALU MERCHANDISERS COMPANY

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

Packages

63941-997-14 — 1 BOTTLE in 1 CARTON (63941-997-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

63941-997-42 — 3 BOTTLE in 1 CARTON (63941-997-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62175-114 — omeprazole, 62175-118 — omeprazole, 62175-136 — omeprazole, 62756-377 — Omeprazole, 63187-061 — Omeprazole, 63187-070 — Omeprazole, 63187-170 — Omeprazole, 63187-805 — Omeprazole, 63187-820 — Omeprazole, 63187-828 — Omeprazole, 63981-915 — Omeprazole, 64380-182 — omeprazole, 64380-183 — omeprazole, 65841-759 — Omeprazole, 65841-760 — Omeprazole, 65841-761 — Omeprazole, 67046-1509 — Omeprazole, 67296-1939 — Omeprazole, 67296-2183 — Omeprazole, 68001-441 — Omeprazole, +295 more

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