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Omeprazole

NDC 63548-7370 · PLD Acquisitions LLC DBA Av�ma Pharma Solutions

Generic nameOmeprazole
Dosage formTABLET, DELAYED RELEASE
RouteORAL
Active ingredient(s)OMEPRAZOLE MAGNESIUM
Strength20.6 mg/1
Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

63548-7370-2 — 1 BOTTLE, PLASTIC in 1 BOX (63548-7370-2) / 42 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

63548-7370-4 — 1 BOTTLE, PLASTIC in 1 BOX (63548-7370-4) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

63548-7370-8 — 1 BOTTLE, PLASTIC in 1 BOX (63548-7370-8) / 28 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57896-759 — Omeprazole Magnesium, 58602-729 — Omeprazole, 58602-826 — Omeprazole, 58602-837 — Omeprazole, 58602-850 — Omeprazole, 59726-298 — Omeprazole, 59726-740 — Omeprazole, 59726-744 — Omeprazole, 63548-2970 — Omeprazole, 63548-4080 — Omeprazole, 63548-8040 — Omeprazole, 63868-177 — Omeprazole Magnesium, 63941-006 — Omeprazole, 66715-6550 — Omeprazole tablet, delayed release, 67091-316 — Omeprazole, 67091-464 — Omeprazole, 68016-760 — Omeprazole Magnesium, 69618-054 — Omeprazole, 69842-027 — Omeprazole Magnesium, 69842-941 — Omeprazole, +56 more

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