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ALPROSTADIL (ALPROSTADIL) — FDA Approval ANDA074815 (HIKMA)

ALPROSTADIL (ALPROSTADIL) — FDA Approval ANDA074815 (HIKMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: ALPROSTADIL; Active ingredients: ALPROSTADIL; Application number: ANDA074815.

Brand nameALPROSTADIL
Active ingredientsALPROSTADIL
Application numberANDA074815
SponsorHIKMA
Dosage formINJECTABLE
RouteINJECTION
Marketing statusPrescription
Products in application1
First approval date19980120
SourceopenFDA Drugs@FDA

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