Visitor Monitoring Drug Details: UNIPEN IN PLASTIC CONTAINER
 
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Drug Details

Drug Name: UNIPEN IN PLASTIC CONTAINER
FDA Application No: (NDA) 050320
Active Ingredient(s): NAFCILLIN SODIUM
Company: WYETH AYERST
Original Approval or Tentative Approval Date: June 23, 1970
 
 
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
UNIPEN NAFCILLIN SODIUMEQ 2GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
UNIPEN NAFCILLIN SODIUMEQ 4GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
UNIPEN NAFCILLIN SODIUMEQ 10GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
UNIPEN NAFCILLIN SODIUMEQ 20GM BASE/VIALINJECTABLE; INJECTION Discontinued No None
UNIPEN NAFCILLIN SODIUMEQ 500MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
UNIPEN IN PLASTIC CONTAINER NAFCILLIN SODIUMEQ 1GM BASE/VIALINJECTABLE; INJECTION Discontinued No None


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