# Allopurinol

NDC: 71205-049
Generic name: ALLOPURINOL
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150429

FDA application: ANDA203154

## Active ingredients

- ALLOPURINOL: 300 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d94f6643-621f-45ed-b2dc-26f84c5626ae