# Prednisone

NDC: 0378-0641
Generic name: Prednisone
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190403

FDA application: ANDA088832

## Active ingredients

- PREDNISONE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-0641"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-0641
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fec09050-5ac2-451b-a2b9-5a21b2def212