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Edex

NDC 52244-040 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic namealprostadil
Labeler / ManufacturerEndo USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA020649
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRACAVERNOUS
Active ingredientsALPROSTADIL (40 ug/mL)
Marketing started20120315
Package count2

External sources

Source: openFDA. Public-domain (CC0).