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ZEGERID

NDC 68012-054 · Santarus, Inc..

Generic nameomeprazole and sodium bicarbonate
Dosage formPOWDER, FOR SUSPENSION
RouteORAL
Active ingredient(s)OMEPRAZOLE, SODIUM BICARBONATE
Strength40; 1680 mg/1; mg/1
Pharmacologic classAlkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryNDA

Packages

68012-054-03 — 3 PACKET in 1 CARTON (68012-054-03) / 1 POWDER, FOR SUSPENSION in 1 PACKET

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65841-759 — Omeprazole, 65841-760 — Omeprazole, 65841-761 — Omeprazole, 67046-1509 — Omeprazole, 67091-108 — ASPIRIN, SODIUM BICARBONATE, CITRIC ACID Tablet, 67296-1939 — Omeprazole, 67296-2183 — Omeprazole, 67751-174 — CITRIC ACID MONOHYDRATE, SODIUM BICARBONATE, 68001-441 — Omeprazole, 68012-052 — omeprazole and sodium bicarbonate, 68012-102 — omeprazole and sodium bicarbonate, 68012-104 — omeprazole and sodium bicarbonate, 68071-2199 — Omeprazole, 68071-2243 — omeprazole, 68071-2262 — Omeprazole, 68071-2741 — Omeprazole, 68071-3007 — Omeprazole, 68071-3733 — Omeprazole, 68071-4024 — Omeprazole, 68071-4025 — 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.