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methylprednisolone

NDC 70771-1350 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206751
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPREDNISOLONE (16 mg/1)
Marketing started20180501
Package count4

External sources

Source: openFDA. Public-domain (CC0).