# Allopurinol

NDC: 0591-5543
Generic name: Allopurinol
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090406
Marketing ended: 20270430
FDA application: NDA018832

## Active ingredients

- ALLOPURINOL: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0591-5543"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0591-5543
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a80fe56f-8d03-423f-8e2a-7ec8c9e5045b