Omeprazole

NDC 60760-747 · St. Mary's Medical Park Pharmacy

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

60760-747-07 — 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-747-07)

60760-747-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-747-30)

60760-747-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-747-60)

60760-747-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-747-90)

FDA lists these products with the same active ingredient.

59651-003 — Omeprazole, 59779-503 — Omeprazole, 59779-580 — Omeprazole, 59779-732 — Omeprazole, sodium bicarbonate, 60505-0065 — Omeprazole, 60505-0145 — Omeprazole, 60505-0146 — Omeprazole, 60505-3952 — Omeprazole, 60687-597 — Omeprazole, 60687-608 — Omeprazole, 60760-833 — Omeprazole, 60760-841 — Omeprazole, 60760-868 — Omeprazole, 62135-530 — Omeprazole, 62135-559 — Omeprazole, 62175-114 — omeprazole, 62175-118 — omeprazole, 62175-136 — omeprazole, 62756-377 — Omeprazole, 63187-061 — 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.