Omeprazole

NDC 69842-661 · CVS Pharmacy

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

69842-661-01 — 1 BOTTLE in 1 CARTON (69842-661-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

69842-661-03 — 3 BOTTLE in 1 CARTON (69842-661-03) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

FDA lists these products with the same active ingredient.

68788-6881 — Omeprazole, 68788-6995 — Omeprazole, 68788-8771 — Omeprazole, 68788-8805 — Omeprazole, 68788-8864 — Omeprazole, 69097-913 — omeprazole sodium bicarbonate, 69097-914 — omeprazole sodium bicarbonate, 69168-476 — Omeprazole, 69230-318 — Omeprazole, 69367-196 — Omeprazole and Sodium Bicarbonate, 69842-791 — omeprazole, 70000-0381 — omeprazole, 70000-0723 — Omeprazole, 70518-0199 — Omeprazole, 70518-2251 — Omeprazole, 70518-3278 — Omeprazole, 70518-4177 — Omeprazole, 70677-0148 — Omeprazole, 70677-1098 — Omeprazole, 70677-1104 — 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.