# PREDNISOLONE

NDC: 60722-5011
Generic name: PREDNISOLONE
Labeler / Manufacturer: Zhejiang Xianju Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240901

FDA application: ANDA218083

## Active ingredients

- PREDNISOLONE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60722-5011"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60722-5011
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52e6e21d-94b8-41a0-8d13-371c0e66bcee