omeprazole
NDC 11822-1190 · Rite Aid Corporation
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
11822-1190-1 — 3 BOTTLE in 1 CARTON (11822-1190-1) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (11822-1190-0)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0781-2785 — Omeprazole, 0781-2790 — Omeprazole, 0781-2859 — Omeprazole, 0781-2868 — Omeprazole, 0904-6917 — Omeprazole, 11673-018 — Omeprazole, 11673-212 — omeprazole, 11673-346 — omeprazole, 11673-915 — Omeprazole, 11822-0453 — Omeprazole, 16714-123 — Omeprazole, 16714-630 — Omeprazole, 16714-634 — Omeprazole, 16714-714 — Omeprazole, 21130-128 — omeprazole, 21130-137 — Omeprazole, 21130-401 — omeprazole, 21130-991 — Omeprazole, 27241-029 — Omeprazole and Sodium Bicarbonate, 27241-030 — Omeprazole and Sodium Bicarbonate, +295 more