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Methylprednisolone Sodium Succinate

NDC 70121-1001 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameMethylprednisolone
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207549
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETHYLPREDNISOLONE SODIUM SUCCINATE (125 mg/2mL)
Marketing started20161111
Package count1

External sources

Source: openFDA. Public-domain (CC0).