Visitor Monitoring Drug Details: SODIUM CHLORIDE
 
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Drug Details

Drug Name: SODIUM CHLORIDE
FDA Application No: (ANDA) 077407
Active Ingredient(s): SODIUM CHLORIDE
Company: TARO PHARMS IRELAND
Original Approval or Tentative Approval Date: August 11, 2006
 
 
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
SODIUM CHLORIDE SODIUM CHLORIDE10MLINJECTABLE; INJECTION Prescription No None
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER SODIUM CHLORIDE9MG/MLINJECTABLE; INJECTION Prescription Yes AP


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