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Omeprazole

NDC 76420-055 · Asclemed USA, Inc.

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

Packages

76420-055-00 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-055-00)

76420-055-03 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-055-03)

76420-055-06 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-055-06)

76420-055-09 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-055-09)

76420-055-10 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-055-10)

76420-055-12 — 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-055-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72288-732 — Omeprazole, sodium bicarbonate, 72288-915 — Omeprazole, 72476-473 — omeprazole, 72559-014 — omeprazole, 72789-155 — omeprazole, 72789-257 — Omeprazole, 72789-482 — Omeprazole, 75907-138 — Omeprazole and Sodium Bicarbonate, 75907-237 — Omeprazole and Sodium Bicarbonate, 76162-470 — omeprazole, 76420-878 — Omeprazole, 76420-879 — Omeprazole, 79481-0075 — omeprazole, 79903-013 — Omeprazole, sodium bicarbonate, 79903-113 — omeprazole, 79903-305 — Omeprazole, 80425-0070 — Omeprazole, 80425-0071 — Omeprazole, 80425-0109 — Omeprazole, 80425-0169 — Omeprazole, +295 more

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