Acid Reducer

NDC 58602-850 · Aurohealth LLC

Generic nameOmeprazole

Dosage formTABLET, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE MAGNESIUM

Strength20 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

58602-850-05 — 1 BOTTLE in 1 CARTON (58602-850-05) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

58602-850-62 — 3 BOTTLE in 1 CARTON (58602-850-62) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE

FDA lists these products with the same active ingredient.

55315-996 — Omeprazole, 55319-037 — Omeprazole, 55319-219 — Omeprazole, 57483-120 — Omeprazole, 57483-740 — omeprazole, 57841-1150 — omeprazole magnesium, amoxicillin and rifabutin, 57896-759 — Omeprazole Magnesium, 58602-729 — Omeprazole, 58602-826 — Omeprazole, 58602-837 — Omeprazole, 59726-298 — Omeprazole, 59726-740 — Omeprazole, 59726-744 — Omeprazole, 63548-2970 — Omeprazole, 63548-4080 — Omeprazole, 63548-7370 — Omeprazole, 63548-8040 — Omeprazole, 63868-177 — Omeprazole Magnesium, 63941-006 — Omeprazole, 66715-6550 — Omeprazole tablet, delayed release, +56 more

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