Omeprazole

NDC 63548-2970 · 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

63548-2970-2 — 1 BOTTLE, PLASTIC in 1 BOX (63548-2970-2) / 42 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

63548-2970-4 — 1 BOTTLE, PLASTIC in 1 BOX (63548-2970-4) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

63548-2970-8 — 1 BOTTLE, PLASTIC in 1 BOX (63548-2970-8) / 28 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC

FDA lists these products with the same active ingredient.

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, 59726-740 — Omeprazole, 59726-744 — 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, 68016-760 — Omeprazole Magnesium, 69618-054 — 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.