Visitor Monitoring Drug Details: DEMECLOCYCLINE HYDROCHLORIDE
 
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Drug Details

Drug Name: DEMECLOCYCLINE HYDROCHLORIDE
FDA Application No: (ANDA) 065171
Active Ingredient(s): DEMECLOCYCLINE HYDROCHLORIDE
Company: BARR
Original Approval or Tentative Approval Date: December 13, 2004
 
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
DEMECLOCYCLINE HYDROCHLORIDE DEMECLOCYCLINE HYDROCHLORIDE150MGTABLET; ORAL Prescription No AB
DEMECLOCYCLINE HYDROCHLORIDE DEMECLOCYCLINE HYDROCHLORIDE300MGTABLET; ORAL Prescription No AB


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