# Allopurinol

NDC: 82638-112
Generic name: Allopurinol
Labeler / Manufacturer: Harman Finochem Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231006

FDA application: ANDA214443

## 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:"82638-112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82638-112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0780dc78-d287-d5db-e063-6294a90aa1dd