Visitor Monitoring Drug Details: DOXEPIN HYDROCHLORIDE
 
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Drug Details

Drug Name: DOXEPIN HYDROCHLORIDE
FDA Application No: (NDA) 016987
Active Ingredient(s): DOXEPIN HYDROCHLORIDE
Company: NEW RIVER
Original Approval or Tentative Approval Date: January 31, 1972
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
DOXEPIN HYDROCHLORIDE DOXEPIN HYDROCHLORIDEEQ 10MG BASECAPSULE; ORAL Discontinued No None
DOXEPIN HYDROCHLORIDE DOXEPIN HYDROCHLORIDEEQ 25MG BASECAPSULE; ORAL Discontinued No None
DOXEPIN HYDROCHLORIDE DOXEPIN HYDROCHLORIDEEQ 50MG BASECAPSULE; ORAL Discontinued No None
DOXEPIN HYDROCHLORIDE DOXEPIN HYDROCHLORIDEEQ 100MG BASECAPSULE; ORAL Discontinued No None
DOXEPIN HYDROCHLORIDE DOXEPIN HYDROCHLORIDEEQ 75MG BASECAPSULE; ORAL Discontinued No None
DOXEPIN HYDROCHLORIDE DOXEPIN HYDROCHLORIDEEQ 150MG BASECAPSULE; ORAL Discontinued No None


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