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MethylPREDNISolone

NDC 55289-649 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemethylprednisolone
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040183
Dosage form / routeTABLET · ORAL
Active ingredientsMETHYLPREDNISOLONE (4 mg/1)
Marketing started19981222
Package count1

External sources

Source: openFDA. Public-domain (CC0).