Omeprazole

NDC 80425-0071 · Advanced Rx of Tennessee, LLC

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

80425-0071-1 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0071-1)

80425-0071-2 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0071-2)

80425-0071-3 — 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0071-3)

FDA lists these products with the same active ingredient.

75907-237 — Omeprazole and Sodium Bicarbonate, 76162-470 — omeprazole, 76420-055 — Omeprazole, 76420-878 — Omeprazole, 76420-879 — Omeprazole, 79481-0075 — omeprazole, 79903-013 — Omeprazole, sodium bicarbonate, 79903-113 — omeprazole, 79903-305 — Omeprazole, 80425-0070 — Omeprazole, 80425-0109 — Omeprazole, 80425-0169 — Omeprazole, 80425-0415 — Omeprazole, 80425-0504 — Omeprazole, 82009-022 — Omeprazole, 82009-023 — Omeprazole, 82009-183 — Omeprazole, 82501-0915 — Omeprazole, 82632-100 — Omeprazole, Sodium Bicarbonate, 82632-699 — omepraole, sodium bicarbonate, +295 more

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