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Methylprednisolone Sodium Succinate

NDC 63323-255 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameMETHYLPREDNISOLONE SODIUM SUCCINATE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040583
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETHYLPREDNISOLONE SODIUM SUCCINATE (40 mg/mL)
Marketing started20041130
Package count1

External sources

Source: openFDA. Public-domain (CC0).