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METHYLPREDNISOLONE ACETATE

NDC 42023-239 · HUMAN PRESCRIPTION DRUG · INJECTION, SUSPENSION

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214297
Dosage form / routeINJECTION, SUSPENSION · INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR SOFT TISSUE
Active ingredientsMETHYLPREDNISOLONE ACETATE (40 mg/mL)
Marketing started20230512
Package count1

External sources

Source: openFDA. Public-domain (CC0).