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Omeprazole delayed release

NDC 49483-731 · TIME CAP LABORATORIES, INC.

Generic nameOmeprazole 20mg
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

49483-731-41 — 3 BOTTLE in 1 CARTON (49483-731-41) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (49483-731-45)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

30142-077 — Omeprazole, 37000-455 — omeprazole magnesium, 37000-459 — OMEPRAZOLE MAGNESIUM, 37808-006 — Omeprazole Magnesium, 37808-569 — Omeprazole, 37835-189 — Omeprazole, 43598-813 — Omeprazole Magnesium, 46122-686 — OMEPRAZOLE, 49035-397 — Omeprazole Magnesium 20.6mg Capsules, 49035-983 — Omeprazole, 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, +56 more

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