Visitor Monitoring Drug Details: SUMYCIN
 
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Drug Details

Drug Name: SUMYCIN
FDA Application No: (ANDA) 061147
Active Ingredient(s): TETRACYCLINE HYDROCHLORIDE
Company: PAR PHARM
Original Approval or Tentative Approval Date: February 10, 1971
 
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
SUMYCIN TETRACYCLINE HYDROCHLORIDE250MGTABLET; ORAL Prescription No None
SUMYCIN TETRACYCLINE HYDROCHLORIDE100MGTABLET; ORAL Discontinued No None
SUMYCIN TETRACYCLINE HYDROCHLORIDE50MGTABLET; ORAL Discontinued No None
SUMYCIN TETRACYCLINE HYDROCHLORIDE500MGTABLET; ORAL Prescription Yes None


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