# PREDNISONE

NDC: 61919-365
Generic name: PREDNISONE
Labeler / Manufacturer: DIRECT RX
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20140101

FDA application: ANDA040584

## 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:"61919-365"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61919-365
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2a053775-6f6a-455e-b9a8-8b60e6062db3