# Allopurinol

NDC: 16714-577
Generic name: Allopurinol
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220701

FDA application: ANDA204467

## 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:"16714-577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=95a1ca8c-9855-4b11-92cd-6fdc144f0d3b