Omeprazole

NDC 30142-593 · Kroger Company

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 categoryNDA

Packages

30142-593-01 — 1 BOTTLE in 1 CARTON (30142-593-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

30142-593-03 — 3 BOTTLE in 1 CARTON (30142-593-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

FDA lists these products with the same active ingredient.

21130-137 — Omeprazole, 21130-401 — omeprazole, 21130-991 — Omeprazole, 27241-029 — Omeprazole and Sodium Bicarbonate, 27241-030 — Omeprazole and Sodium Bicarbonate, 27241-031 — Omeprazole and Sodium Bicarbonate, 27241-032 — Omeprazole and Sodium Bicarbonate, 30142-394 — omeprazole, 30142-474 — omeprazole, 30142-557 — Omeprazole, 30142-992 — omeprazole, 31722-527 — omeprazole, 31722-528 — omeprazole, 36800-121 — Omeprazole, 36800-601 — omeprazole, 36800-915 — Omeprazole, 37808-354 — omeprazole, 37808-401 — Omeprazole, 37808-732 — Omeprazole, sodium bicarbonate, 37808-915 — 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.