FDA Drug Approval, N019815, PROAMATINE

FDA Drug Approval, N019815, PROAMATINE

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NDA: 019815
Company: TAKEDA PHARMS USA
Drug Name: PROAMATINE
Active Ingredients: MIDODRINE HYDROCHLORIDE
Strength: 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage Form/Route: TABLET;ORAL
Action Date: 09/06/1996
Marketing Status: Discontinued
Submission Classification: Type 1 - New Molecular Entity

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