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Methylprednisolone Sodium Succinate

NDC 55150-265 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerEugia US LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA207667
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETHYLPREDNISOLONE SODIUM SUCCINATE (2 g/1)
Marketing started20151215
Package count1

External sources

Source: openFDA. Public-domain (CC0).