Visitor Monitoring Drug Details: SUMYCIN
 
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Drug Details

Drug Name: SUMYCIN
FDA Application No: (ANDA) 060429
Active Ingredient(s): TETRACYCLINE HYDROCHLORIDE
Company: APOTHECON
Original Approval or Tentative Approval Date: September 17, 1954
 
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 HYDROCHLORIDE250MGCAPSULE; ORAL Discontinued No None
SUMYCIN TETRACYCLINE HYDROCHLORIDE100MGCAPSULE; ORAL Discontinued No None
SUMYCIN TETRACYCLINE HYDROCHLORIDE500MGCAPSULE; ORAL Discontinued No None
SUMYCIN TETRACYCLINE HYDROCHLORIDE125MGCAPSULE; ORAL Discontinued No None


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