# Prednisone

NDC: 76420-069
Generic name: Prednisone
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20010829

FDA application: ANDA040362

## 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:"76420-069"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-069
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc663fd3-b149-48ae-a3f3-6abaa4808cc6