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Omeprazole

NDC 83324-011 · CHAIN DRUG MARKETING ASSOCIATION, INC.

Generic nameOmeprazole
Dosage formTABLET, 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

83324-011-14 — 1 CONTAINER in 1 CARTON (83324-011-14) / 14 TABLET, DELAYED RELEASE in 1 CONTAINER

83324-011-42 — 3 CONTAINER in 1 CARTON (83324-011-42) / 14 TABLET, DELAYED RELEASE in 1 CONTAINER

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

82009-023 — Omeprazole, 82009-183 — Omeprazole, 82501-0915 — Omeprazole, 82632-100 — Omeprazole, Sodium Bicarbonate, 82632-699 — omepraole, sodium bicarbonate, 82725-4052 — Omeprazole 20mg, 82804-166 — Omeprazole, 82804-280 — Omeprazole, 82868-043 — Omeprazole, 82868-080 — Omeprazole, 83209-150 — Omeprazole, 83324-141 — Omeprazole, 85509-1031 — Omeprazole and Sodium Bicarbonate, 85509-1032 — Omeprazole and Sodium Bicarbonate, 85509-1396 — Omeprazole, 85509-1644 — Omeprazole, 85534-0036 — Omeprazole, 85534-0037 — Omeprazole, 85534-0064 — Omeprazole, 87441-063 — 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.