# METHYLPREDNISOLONE ACETATE

NDC: 42023-239
Generic name: METHYLPREDNISOLONE ACETATE
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SUSPENSION
Routes: INTRA-ARTICULAR, INTRALESIONAL, INTRAMUSCULAR, SOFT TISSUE
Marketing started: 20230512

FDA application: ANDA214297

## Active ingredients

- METHYLPREDNISOLONE ACETATE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42023-239"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-239
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=631f7d3e-5620-4be3-b918-2f0d38a97890