# Allopurinol

NDC: 55111-730
Generic name: allopurinol
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20091001

FDA application: ANDA071587

## 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:"55111-730"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-730
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=19a138b8-d225-03e6-f762-abe71560204b