Visitor Monitoring Drug Details: AMIODARONE HYDROCHLORIDE
 
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Drug Details

Drug Name: AMIODARONE HYDROCHLORIDE
FDA Application No: (ANDA) 076362
Active Ingredient(s): AMIODARONE HYDROCHLORIDE
Company: TARO
Original Approval or Tentative Approval Date: November 29, 2002
 
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
AMIODARONE HYDROCHLORIDE AMIODARONE HYDROCHLORIDE400MGTABLET; ORAL Prescription No AB
AMIODARONE HYDROCHLORIDE AMIODARONE HYDROCHLORIDE300MGTABLET; ORAL Prescription No None


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