Visitor Monitoring Drug Details: TERAZOSIN HYDROCHLORIDE
 
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Drug Details

Drug Name: TERAZOSIN HYDROCHLORIDE
FDA Application No: (ANDA) 074823
Active Ingredient(s): TERAZOSIN HYDROCHLORIDE
Company: SANDOZ
Original Approval or Tentative Approval Date: March 30, 1998
 
Therapeutic Equivalents Labels are not available
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
TERAZOSIN HYDROCHLORIDE TERAZOSIN HYDROCHLORIDEEQ 1MG BASECAPSULE; ORAL Prescription No AB
TERAZOSIN HYDROCHLORIDE TERAZOSIN HYDROCHLORIDEEQ 2MG BASECAPSULE; ORAL Prescription No AB
TERAZOSIN HYDROCHLORIDE TERAZOSIN HYDROCHLORIDEEQ 5MG BASECAPSULE; ORAL Prescription No AB
TERAZOSIN HYDROCHLORIDE TERAZOSIN HYDROCHLORIDEEQ 10MG BASECAPSULE; ORAL Prescription No AB


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