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SODIUM BICARBONATE

NDC 68462-951 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA219701
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSODIUM BICARBONATE (84 mg/mL)
Marketing started20250807
Package count1

External sources

Source: openFDA. Public-domain (CC0).