# Prednisone

NDC: 70882-117
Generic name: Prednisone
Labeler / Manufacturer: Cambridge Therapeutics Technologies, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20010829

FDA application: ANDA040362

## 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:"70882-117"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70882-117
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d6246d5f-bf2b-4850-978e-6ea3148de095