# Allopurinol

NDC: 70518-3660
Generic name: Allopurinol
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230224

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:"70518-3660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=36526c80-5a70-47c4-a0a6-785ccc346703