# Allopurinol

NDC: 0378-0181
Generic name: allopurinol
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19861024

FDA application: ANDA018659

## 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:"0378-0181"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-0181
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bdbf5ad4-86f2-4e9c-a51a-fb0c7220c480