Visitor Monitoring Drug Details: MANNITOL 10% IN PLASTIC CONTAINER
 
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Drug Details

Drug Name: MANNITOL 10% IN PLASTIC CONTAINER
FDA Application No: (NDA) 020006
Active Ingredient(s): MANNITOL
Company: B BRAUN
Original Approval or Tentative Approval Date: July 26, 1993
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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% IN PLASTIC CONTAINER MANNITOL10GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 15% IN PLASTIC CONTAINER MANNITOL15GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 20% IN PLASTIC CONTAINER MANNITOL20GM/100MLINJECTABLE; INJECTION Prescription No AP
MANNITOL 5% IN PLASTIC CONTAINER MANNITOL5GM/100MLINJECTABLE; INJECTION Prescription No AP


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