Visitor Monitoring Drug Details: MANNITOL 5%
 
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Drug Details

Drug Name: MANNITOL 5%
FDA Application No: (NDA) 016269
Active Ingredient(s): MANNITOL
Company: HOSPIRA
Original Approval or Tentative Approval Date: December 22, 1967
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
MANNITOL 10% MANNITOL10GM/100MLINJECTABLE; INJECTION Discontinued No None
MANNITOL 15% MANNITOL15GM/100MLINJECTABLE; INJECTION Discontinued No None
MANNITOL 20% MANNITOL20GM/100MLINJECTABLE; INJECTION Discontinued No None
MANNITOL 25% MANNITOL12.5GM/50MLINJECTABLE; INJECTION Discontinued No None
MANNITOL 25% MANNITOL12.5GM/50MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 5% MANNITOL5GM/100MLINJECTABLE; INJECTION Discontinued No None


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