Visitor Monitoring Drug Details: SECTRAL
 
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Drug Details

Drug Name: SECTRAL
FDA Application No: (NDA) 018917
Active Ingredient(s): ACEBUTOLOL HYDROCHLORIDE
Company: DR REDDYS LABS INC
Original Approval or Tentative Approval Date: December 28, 1984
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SECTRAL ACEBUTOLOL HYDROCHLORIDEEQ 200MG BASECAPSULE; ORAL Prescription No AB
SECTRAL ACEBUTOLOL HYDROCHLORIDEEQ 400MG BASECAPSULE; ORAL Prescription Yes AB


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