# Prednisone D/P

NDC: 72189-673
Generic name: Prednisone D/P
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260409

FDA application: ANDA211575

## 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:"72189-673"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-673
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f0a3946-025c-798a-e063-6294a90a831b