# Prednisone delayed release

NDC: 74157-019
Generic name: Prednisone
Labeler / Manufacturer: INA Pharmaceutics Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20251215

FDA application: ANDA219477

## Active ingredients

- PREDNISONE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"74157-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=74157-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=463c7cd2-c973-5c6c-e063-6394a90a09a0