Visitor Monitoring Drug Details: OCL
 
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Drug Details

Drug Name: OCL
FDA Application No: (NDA) 019284
Active Ingredient(s): POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE
Company: HOSPIRA
Original Approval or Tentative Approval Date: April 30, 1986
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
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
OCL POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE6GM/100ML; 75MG/100ML; 168MG/100ML; 146MG/100ML; 1.29GM/100MLSOLUTION; ORAL Discontinued No None


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