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Omeprazole and Sodium Bicarbonate

NDC 70954-797 · ANI Pharmaceuticals, Inc.

Generic nameOmeprazole and Sodium Bicarbonate
Dosage formPOWDER, FOR SUSPENSION
RouteORAL
Active ingredient(s)OMEPRAZOLE, SODIUM BICARBONATE
Strength20; 1680 mg/1; mg/1
Pharmacologic classAlkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

70954-797-20 — 30 PACKET in 1 CARTON (70954-797-20) / 1 POWDER, FOR SUSPENSION in 1 PACKET (70954-797-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70677-0148 — Omeprazole, 70677-1098 — Omeprazole, 70677-1104 — Omeprazole, 70677-1275 — Omeprazole, 70700-149 — Omeprazole, 70700-150 — Omeprazole, 70700-151 — Omeprazole, 70708-110 — NASAL WASH, 70708-210 — NASAL WASH, 70795-1190 — Sodium Bicarbonate, 70954-798 — Omeprazole and Sodium Bicarbonate, 71205-157 — omeprazole, 71205-501 — Omeprazole, 71205-613 — Omeprazole, 71205-907 — Omeprazole, 71205-985 — Omeprazole and Sodium Bicarbonate, 71335-0299 — Omeprazole, 71335-0332 — Omeprazole, 71335-0569 — Omeprazole, 71335-1395 — Omeprazole, +494 more

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