Omeprazole

NDC 85534-0036 · HAWAII REPACK, 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

85534-0036-0 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0036-0)

85534-0036-1 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0036-1)

85534-0036-2 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0036-2)

85534-0036-3 — 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0036-3)

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, 83324-011 — Omeprazole, 83324-141 — Omeprazole, 85509-1031 — Omeprazole and Sodium Bicarbonate, 85509-1032 — Omeprazole and Sodium Bicarbonate, 85509-1396 — Omeprazole, 85509-1644 — Omeprazole, 85534-0037 — Omeprazole, 85534-0064 — Omeprazole, 87441-063 — Omeprazole, +295 more

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