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omeprazole

NDC 57483-740 · INNOVUS PHARMACEUTICALS, INC.

Generic nameomeprazole
Dosage formCAPSULE, 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

57483-740-42 — 3 BOTTLE in 1 CARTON (57483-740-42) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57483-740-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51316-061 — Omeprazole, 51316-271 — Omeprazole magnesium, 51316-843 — Omeprazole, 53943-016 — Omeprazole, 53943-520 — Omeprazole Magnesium, 55111-397 — Omeprazole Magnesium, 55315-996 — Omeprazole, 55319-037 — Omeprazole, 55319-219 — Omeprazole, 57483-120 — 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, 63548-2970 — 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.