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Methylprednisolone Sodium Succinate

NDC 0143-9850 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202691
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMETHYLPREDNISOLONE SODIUM SUCCINATE (500 mg/1)
Marketing started20160101
Package count1

External sources

Source: openFDA. Public-domain (CC0).