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Dextrose

NDC 63323-624 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameDextrose Monohydrate
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207449
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXTROSE MONOHYDRATE (50 mg/mL)
Marketing started20161021
Package count5

External sources

Source: openFDA. Public-domain (CC0).