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Methylprednisolone Sodium Succinate

NDC 70518-4345 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA203125
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETHYLPREDNISOLONE SODIUM SUCCINATE (125 mg/1)
Marketing started20250527
Package count1

External sources

Source: openFDA. Public-domain (CC0).