# Prednisone

NDC: 51655-197
Generic name: Prednisone
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230425

FDA application: ANDA040581

## Active ingredients

- PREDNISONE: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-197"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-197
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=faf6c0c5-e5f4-4de5-e053-6294a90abd1a