# Prednisone

NDC: 60687-145
Generic name: Prednisone
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151005
Marketing ended: 20270331
FDA application: ANDA040392

## Active ingredients

- PREDNISONE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60687-145"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-145
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0e8d1a2-8c82-4dc0-8c2f-9da84382f34e