# prednisone

NDC: 70518-3401
Generic name: PREDNISONE
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220405

FDA application: ANDA208412

## Active ingredients

- PREDNISONE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3401"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3401
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af5d0f73-2aef-4db1-ae25-6d465c9f0ca1