FDA Drug Approval, N018917, SECTRAL

FDA Drug Approval, N018917, SECTRAL

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NDA: 018917
Company: PROMIUS PHARMA
Drug Name: SECTRAL
Active Ingredients: ACEBUTOLOL HYDROCHLORIDE
Strength: CAPSULE;ORAL
Dosage Form/Route: Discontinued
Action Date: ORIG-1
Marketing Status: None
Submission Classification: STANDARD

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