Visitor Monitoring Drug Details: UNASYN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: UNASYN
FDA Application No: (NDA) 050608
Active Ingredient(s): AMPICILLIN SODIUM; SULBACTAM SODIUM
Company: PFIZER
Original Approval or Tentative Approval Date: December 31, 1986
Chemical Type: 14 New molecular entity and new combination
Review Classification: S Standard review drug
 
There are no 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
UNASYN AMPICILLIN SODIUM; SULBACTAM SODIUMEQ 2GM BASE/VIAL; EQ 1GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
UNASYN AMPICILLIN SODIUM; SULBACTAM SODIUMEQ 1GM BASE/VIAL; EQ 500MG BASE/VIALINJECTABLE; INJECTION Prescription Yes AP
UNASYN AMPICILLIN SODIUM; SULBACTAM SODIUMEQ 500MG BASE/VIAL; EQ 250MG BASE/VIALINJECTABLE; INJECTION Discontinued No None
UNASYN AMPICILLIN SODIUM; SULBACTAM SODIUMEQ 10GM BASE/VIAL; EQ 5GM BASE/VIALINJECTABLE; INJECTION Prescription Yes AP


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