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Aloprim

NDC 67457-187 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameAllopurinol
Labeler / ManufacturerMylan Institutional LLC
Marketing categoryNew Drug Application (innovator) · App NDA020298
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsALLOPURINOL SODIUM (500 mg/25mL)
Marketing started20070515
Package count1

External sources

Source: openFDA. Public-domain (CC0).