Visitor Monitoring Drug Details: MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12%
 
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Drug Details

Drug Name: MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12%
FDA Application No: (NDA) 016080
Active Ingredient(s): MANNITOL
Company: B BRAUN
Original Approval or Tentative Approval Date: October 8, 1965
Chemical Type: 5 New manufacturer
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
MANNITOL 10% MANNITOL10GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 10% W/ DEXTROSE 5% IN DISTILLED WATER MANNITOL10GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 15% MANNITOL15GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 15% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.45% MANNITOL15GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 20% MANNITOL20GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 5% MANNITOL5GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 5% W/ DEXTROSE 5% IN SODIUM CHLORIDE 0.12% MANNITOL5GM/100MLINJECTABLE; INJECTION Prescription No AP


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