equate omeprazole

NDC 79903-113 · WALMART 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 categoryNDA

Packages

79903-113-42 — 3 BOTTLE in 1 CARTON (79903-113-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79903-113-14)

FDA lists these products with the same active ingredient.

72789-257 — Omeprazole, 72789-482 — Omeprazole, 75907-138 — Omeprazole and Sodium Bicarbonate, 75907-237 — Omeprazole and Sodium Bicarbonate, 76162-470 — omeprazole, 76420-055 — Omeprazole, 76420-878 — Omeprazole, 76420-879 — Omeprazole, 79481-0075 — omeprazole, 79903-013 — Omeprazole, sodium bicarbonate, 79903-305 — Omeprazole, 80425-0070 — Omeprazole, 80425-0071 — Omeprazole, 80425-0109 — Omeprazole, 80425-0169 — Omeprazole, 80425-0415 — Omeprazole, 80425-0504 — Omeprazole, 82009-022 — Omeprazole, 82009-023 — Omeprazole, 82009-183 — 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.