Omeprazole

NDC 70677-1098 · STRATEGIC SOURCING SERVICES LLC

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

70677-1098-1 — 1 BLISTER PACK in 1 CARTON (70677-1098-1) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

69367-196 — Omeprazole and Sodium Bicarbonate, 69842-661 — omeprazole, 69842-791 — omeprazole, 70000-0381 — omeprazole, 70000-0723 — Omeprazole, 70518-0199 — Omeprazole, 70518-2251 — Omeprazole, 70518-3278 — Omeprazole, 70518-4177 — Omeprazole, 70677-0148 — Omeprazole, 70677-1104 — Omeprazole, 70677-1275 — Omeprazole, 70700-149 — Omeprazole, 70700-150 — Omeprazole, 70700-151 — Omeprazole, 70954-797 — Omeprazole and Sodium Bicarbonate, 70954-798 — Omeprazole and Sodium Bicarbonate, 71205-157 — omeprazole, 71205-501 — Omeprazole, 71205-613 — 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.