Visitor Monitoring Drug Details: ROBITET
 
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Drug Details

Drug Name: ROBITET
FDA Application No: (ANDA) 061734
Active Ingredient(s): TETRACYCLINE HYDROCHLORIDE
Company: WYETH AYERST
 
Therapeutic Equivalents Labels are not available
Approval History and Related Documents are not available
 
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
ROBITET TETRACYCLINE HYDROCHLORIDE250MGCAPSULE; ORAL Discontinued No None
ROBITET TETRACYCLINE HYDROCHLORIDE500MGCAPSULE; ORAL Discontinued No None


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