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omeprazole

NDC 72559-014 · Little Pharma, 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

72559-014-06 — 3 BOTTLE in 1 CARTON (72559-014-06) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

72559-014-07 — 1 BOTTLE in 1 CARTON (72559-014-07) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

72559-014-09 — 3 CARTON in 1 PACKAGE, COMBINATION (72559-014-09) / 3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

72559-014-36 — 4 CARTON in 1 PACKAGE, COMBINATION (72559-014-36) / 3 BOTTLE in 1 CARTON / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-1906 — omeprazole, sodium bicarbonate, 72162-2388 — Omeprazole, 72189-568 — Omeprazole/Sodiium Bicarbonate, 72288-047 — omeprazole, 72288-123 — omeprazole, 72288-401 — Omeprazole, 72288-606 — Omeprazole, 72288-732 — Omeprazole, sodium bicarbonate, 72288-915 — Omeprazole, 72476-473 — omeprazole, 72789-155 — omeprazole, 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, +295 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.