# Prednisone delayed release

NDC: 43598-888
Generic name: Prednisone
Labeler / Manufacturer: Dr. Reddys Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260812

FDA application: ANDA218035

## 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:"43598-888"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-888
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=474974ac-9811-c9f5-4050-58e535351d00