Visitor Monitoring Drug Details: CYCLOPAR
 
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Drug Details

Drug Name: CYCLOPAR
FDA Application No: (ANDA) 061725
Active Ingredient(s): TETRACYCLINE HYDROCHLORIDE
Company: WARNER CHILCOTT
Original Approval or Tentative Approval Date: June 8, 1973
 
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
CYCLOPAR TETRACYCLINE HYDROCHLORIDE250MGCAPSULE; ORAL Discontinued No None
CYCLOPAR TETRACYCLINE HYDROCHLORIDE500MGCAPSULE; ORAL Discontinued No None


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