Omeprazole

NDC 62756-377 · Sun Pharmaceutical Industries, Inc.

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

62756-377-11 — 2 BOTTLE in 1 CARTON (62756-377-11) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

62756-377-12 — 3 BOTTLE in 1 CARTON (62756-377-12) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

62756-377-21 — 1 BOTTLE in 1 CARTON (62756-377-21) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

62756-377-70 — 1 BLISTER PACK in 1 CARTON (62756-377-70) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

62756-377-79 — 3 BLISTER PACK in 1 CARTON (62756-377-79) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

62756-377-96 — 2 BLISTER PACK in 1 CARTON (62756-377-96) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

60687-608 — Omeprazole, 60760-747 — 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, 63187-061 — Omeprazole, 63187-070 — Omeprazole, 63187-170 — Omeprazole, 63187-805 — Omeprazole, 63187-820 — Omeprazole, 63187-828 — Omeprazole, 63941-997 — Omeprazole, 63981-915 — Omeprazole, 64380-182 — omeprazole, 64380-183 — 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.