# ALLOPURINOL

NDC: 72189-417
Generic name: ALLOPURINOL
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230202
Marketing ended: 20291031
FDA application: ANDA204467

## Active ingredients

- ALLOPURINOL: 300 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-417"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-417
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3bd5852-8e43-6b5d-e053-2995a90a194f