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Dextrose monohydrate

NDC 51662-1584 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA203451
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsDEXTROSE MONOHYDRATE (25 g/50mL)
Marketing started20220211
Package count2

External sources

Source: openFDA. Public-domain (CC0).