# Allopurinol

NDC: 67544-736
Generic name: allopurinol
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19861024

FDA application: ANDA018659

## 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:"67544-736"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67544-736
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae821c68-626a-474c-b81d-ce75d9795b3c