omeprazole

NDC 59640-047 · H E B

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

59640-047-03 — 3 BOTTLE in 1 CARTON (59640-047-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (59640-047-01)

FDA lists these products with the same active ingredient.

55910-713 — omeprazole, 55910-915 — Omeprazole, 56062-401 — Omeprazole, 56062-915 — Omeprazole, 57237-160 — Omeprazole, 57237-161 — Omeprazole, 57237-162 — Omeprazole, 57483-840 — omeprazole, 57896-659 — Omeprazole, 58602-725 — OMEPRAZOLE AND SODIUM BICARBONATE, 59640-699 — Omeprazole, 59651-001 — Omeprazole, 59651-002 — Omeprazole, 59651-003 — Omeprazole, 59779-503 — Omeprazole, 59779-580 — Omeprazole, 59779-732 — Omeprazole, sodium bicarbonate, 60505-0065 — Omeprazole, 60505-0145 — Omeprazole, 60505-0146 — 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.