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Omeprazole

NDC 59726-740 · P & L Development, 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

59726-740-42 — 3 BOTTLE, PLASTIC in 1 BOX (59726-740-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 58602-850 — Omeprazole, 59726-298 — 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, 67091-316 — Omeprazole, 67091-464 — Omeprazole, +56 more

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