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Ascorbic Acid

NDC 65219-027 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217131
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsASCORBIC ACID (500 mg/mL)
Marketing started20251208
Package count2

External sources

Source: openFDA. Public-domain (CC0).