Visitor Monitoring Drug Details: SALPIX
 
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Drug Details

Drug Name: SALPIX
FDA Application No: (NDA) 009008
Active Ingredient(s): ACETRIZOATE SODIUM
Company: ORTHO MCNEIL PHARM
Chemical Type: 4 New combination
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History and Related Documents are not available
 
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
SALPIX ACETRIZOATE SODIUM53%SOLUTION; INTRAUTERINE Discontinued No None


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