# Aloprim

NDC: 67457-187
Generic name: Allopurinol
Labeler / Manufacturer: Mylan Institutional LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20070515

FDA application: NDA020298

## Active ingredients

- ALLOPURINOL SODIUM: 500 mg/25mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67457-187"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67457-187
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=10cc918f-aa44-415b-932d-2404695ac449