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DROXIDOPA (DROXIDOPA) — FDA Approval ANDA214384 (SUN PHARM)

DROXIDOPA (DROXIDOPA) — FDA Approval ANDA214384 (SUN PHARM) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DROXIDOPA; Active ingredients: DROXIDOPA; Application number: ANDA214384.

Brand nameDROXIDOPA
Active ingredientsDROXIDOPA
Application numberANDA214384
SponsorSUN PHARM
Dosage formCAPSULE
RouteORAL
Marketing statusPrescription
Products in application3
First approval date20210218
SourceopenFDA Drugs@FDA

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