# Prednisone

NDC: 66267-172
Generic name: Prednisone
Labeler / Manufacturer: NuCare Pharmaceuticals,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: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66267-172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66267-172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63102d75-9b2b-84a9-e053-2a91aa0a317d