# MethylPREDNISolone

NDC: 0603-4593
Generic name: methylprednisolone
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19981222

FDA application: ANDA040183

## Active ingredients

- METHYLPREDNISOLONE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0603-4593"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0603-4593
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c84cf5e6-746d-41fb-b3d8-2c0b8ba989af