# Allopurinol

NDC: 29300-349
Generic name: Allopurinol
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190312

FDA application: ANDA211820

## Active ingredients

- ALLOPURINOL: 100 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-349"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-349
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e3face45-f920-46a0-b707-6a66aa9735bd