# Allopurinol

NDC: 43063-934
Generic name: Allopurinol
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19870109

FDA application: ANDA071450

## 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:"43063-934"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-934
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f1c11f74-1de2-484c-b40b-d0013e8fd01a