omeprazole

NDC 72288-606 · Amazon.com Services LLC

Generic nameOmeprazole

Dosage formCAPSULE, 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

72288-606-03 — 3 BOTTLE in 1 CARTON (72288-606-03) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72288-606-01)

FDA lists these products with the same active ingredient.

71610-912 — Omeprazole, 71610-942 — Omeprazole, 71610-963 — Omeprazole, 72036-981 — OMEPRAZOLE, 72162-1906 — omeprazole, sodium bicarbonate, 72162-2388 — Omeprazole, 72189-568 — Omeprazole/Sodiium Bicarbonate, 72288-047 — omeprazole, 72288-123 — omeprazole, 72288-401 — Omeprazole, 72288-732 — Omeprazole, sodium bicarbonate, 72288-915 — Omeprazole, 72476-473 — omeprazole, 72559-014 — 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, +295 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.