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Calcium Gluconate

NDC 65219-162 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryNew Drug Application (innovator) · App NDA208418
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsCALCIUM GLUCONATE MONOHYDRATE (20 mg/mL)
Marketing started20210617
Package count1

External sources

Source: openFDA. Public-domain (CC0).