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Omeprazole

NDC 57237-161 · Rising Pharma Holdings, Inc.

Generic nameOmeprazole
Dosage formCAPSULE, 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

57237-161-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-01)

57237-161-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-30)

57237-161-50 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-50)

57237-161-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-90)

57237-161-99 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-2332 — Omeprazole, 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, 57237-162 — 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, +295 more

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