# Allopurinol

NDC: 71921-241
Generic name: Allopurinol
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250522

FDA application: ANDA204467

## Active ingredients

- ALLOPURINOL: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71921-241"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-241
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=815af471-5985-4819-936d-1f5f3d871ef8