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24 hr omeprazole

NDC 79481-0075 · Meijer, 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 categoryNDA

Packages

79481-0075-1 — 14 TABLET, DELAYED RELEASE in 1 BOTTLE (79481-0075-1)

79481-0075-3 — 3 BOTTLE in 1 CARTON (79481-0075-3) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 76420-055 — Omeprazole, 76420-878 — Omeprazole, 76420-879 — Omeprazole, 79903-013 — Omeprazole, sodium bicarbonate, 79903-113 — omeprazole, 79903-305 — Omeprazole, 80425-0070 — Omeprazole, 80425-0071 — Omeprazole, 80425-0109 — Omeprazole, 80425-0169 — Omeprazole, 80425-0415 — Omeprazole, 80425-0504 — Omeprazole, 82009-022 — 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.