# ALLOPURINOL

NDC: 31722-252
Generic name: ALLOPURINOL
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230803

FDA application: ANDA217748

## Active ingredients

- ALLOPURINOL: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-252"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-252
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=60750373-7146-455a-8d12-d0e32d2d4bc8