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Omeprazole/Sodiium Bicarbonate

NDC 72189-568 · Direct_rx

Generic nameOmeprazole/Sodiium Bicarbonate
Dosage formCAPSULE
RouteORAL
Active ingredient(s)OMEPRAZOLE, SODIUM BICARBONATE
Strength40; 1100 mg/1; mg/1
Pharmacologic classAlkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
Marketing categoryANDA

Packages

72189-568-30 — 30 CAPSULE in 1 BOTTLE (72189-568-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71872-7097 — Sodium Bicarbonate, 71872-7247 — SODIUM BICARBONATE, 71872-7266 — Sodium Bicarbonate, 71872-7310 — SODIUM BICARBONATE, 71872-7371 — SODIUM BICARBONATE, 71872-7376 — SODIUM BICARBONATE, 72036-981 — OMEPRAZOLE, 72162-1906 — omeprazole, sodium bicarbonate, 72162-2314 — SODIUM BICARBONATE, 72162-2388 — Omeprazole, 72288-047 — omeprazole, 72288-123 — omeprazole, 72288-401 — Omeprazole, 72288-606 — Omeprazole, 72288-732 — Omeprazole, sodium bicarbonate, 72288-915 — Omeprazole, 72476-473 — omeprazole, 72559-014 — omeprazole, 72572-200 — Sodium Bicarbonate, injection, 72572-740 — SODIUM BICARBONATE, +494 more

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