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Dexamethasone Sodium Phosphate

NDC 76045-212 · HUMAN PRESCRIPTION DRUG · INJECTION, EMULSION

Generic nameDEXAMETHASONE SODIUM PHOSPHATE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209192
Dosage form / routeINJECTION, EMULSION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsDEXAMETHASONE SODIUM PHOSPHATE (10 mg/mL)
Marketing started20240221
Package count1

External sources

Source: openFDA. Public-domain (CC0).