# Allopurinol

NDC: 68788-8458
Generic name: Allopurinol
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230614

FDA application: ANDA211820

## 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:"68788-8458"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8458
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e11e94b9-d897-48ce-9a80-aa6b8b5fde02