up and up omeprazole
NDC 11673-212 · Target Corporation
Generic nameomeprazole
Dosage formTABLET, ORALLY DISINTEGRATING, 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
11673-212-55 — 3 CARTON in 1 CARTON (11673-212-55) / 14 BLISTER PACK in 1 CARTON / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0536-1448 — Omeprazole, 0615-8079 — Omeprazole, 0615-8406 — Omeprazole, 0781-2234 — Omeprazole, 0781-2785 — Omeprazole, 0781-2790 — Omeprazole, 0781-2859 — Omeprazole, 0781-2868 — Omeprazole, 0904-6917 — Omeprazole, 11673-018 — Omeprazole, 11673-346 — omeprazole, 11673-915 — Omeprazole, 11822-0453 — Omeprazole, 11822-1190 — omeprazole, 16714-123 — Omeprazole, 16714-630 — Omeprazole, 16714-634 — Omeprazole, 16714-714 — Omeprazole, 21130-128 — omeprazole, 21130-137 — Omeprazole, +295 more