Omeprazole

NDC 57237-162 · Rising Pharma Holdings, Inc.

Generic nameOmeprazole

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE

Strength40 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

57237-162-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-01)

57237-162-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-10)

57237-162-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-30)

57237-162-50 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-50)

57237-162-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-162-90)

FDA lists these products with the same active ingredient.

55301-915 — Omeprazole, 55681-306 — OMEPRAZOLE, 55910-215 — Omeprazole, 55910-712 — omeprazole, 55910-713 — omeprazole, 55910-915 — Omeprazole, 56062-401 — Omeprazole, 56062-915 — Omeprazole, 57237-160 — Omeprazole, 57237-161 — Omeprazole, 57483-840 — omeprazole, 57896-659 — Omeprazole, 58602-725 — OMEPRAZOLE AND SODIUM BICARBONATE, 59640-047 — omeprazole, 59640-699 — Omeprazole, 59651-001 — Omeprazole, 59651-002 — Omeprazole, 59651-003 — Omeprazole, 59779-503 — Omeprazole, 59779-580 — 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.