Omeprazole

NDC 68001-441 · BluePoint Laboratories

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

68001-441-39 — 2 BOTTLE in 1 CARTON (68001-441-39) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)

68001-441-40 — 3 BOTTLE in 1 CARTON (68001-441-40) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)

68001-441-98 — 1 BOTTLE in 1 CARTON (68001-441-98) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)

FDA lists these products with the same active ingredient.

63941-997 — 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, 68012-052 — omeprazole and sodium bicarbonate, 68012-054 — omeprazole and sodium bicarbonate, 68012-102 — omeprazole and sodium bicarbonate, 68012-104 — omeprazole and sodium bicarbonate, 68071-2199 — Omeprazole, 68071-2243 — omeprazole, 68071-2262 — Omeprazole, 68071-2741 — Omeprazole, 68071-3007 — Omeprazole, 68071-3733 — Omeprazole, +295 more

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