# Allopurinol

NDC: 53489-156
Generic name: Allopurinol
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19870109

FDA application: ANDA071450

## Active ingredients

- ALLOPURINOL: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53489-156"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53489-156
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd8f8b8b-f25e-46e9-969a-65363b66e09b