Strength
100 ug/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
63304008690
Classification
Generic
Dosage Form
CAPSULE
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
DROXIDOPAApproval Type
Generic (ANDA)
FDA Application
ANDA214384On Market Since
2/18/2021
Pharmacological Classes
Catecholamines
Increased Blood Pressure
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