Visitor Monitoring Drug Details: SINEQUAN
 
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Drug Details

Drug Name: SINEQUAN
FDA Application No: (NDA) 016798
Active Ingredient(s): DOXEPIN HYDROCHLORIDE
Company: PFIZER
Original Approval or Tentative Approval Date: September 23, 1969
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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
SINEQUAN DOXEPIN HYDROCHLORIDEEQ 25MG BASECAPSULE; ORAL Prescription Yes AB
SINEQUAN DOXEPIN HYDROCHLORIDEEQ 50MG BASECAPSULE; ORAL Prescription No AB
SINEQUAN DOXEPIN HYDROCHLORIDEEQ 10MG BASECAPSULE; ORAL Prescription No AB
SINEQUAN DOXEPIN HYDROCHLORIDEEQ 100MG BASECAPSULE; ORAL Prescription Yes AB
SINEQUAN DOXEPIN HYDROCHLORIDEEQ 75MG BASECAPSULE; ORAL Prescription No AB
SINEQUAN DOXEPIN HYDROCHLORIDEEQ 150MG BASECAPSULE; ORAL Prescription No AB


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