Visitor Monitoring Drug Details: K+8
 
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Drug Details

Drug Name: K+8
FDA Application No: (ANDA) 070998
Active Ingredient(s): POTASSIUM CHLORIDE
Company: ALRA
Original Approval or Tentative Approval Date: January 25, 1993
 
 
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
K+8 POTASSIUM CHLORIDE8MEQTABLET, EXTENDED RELEASE; ORAL Prescription No AB


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