Visitor Monitoring Drug Details: OSMITROL 15% IN WATER IN PLASTIC CONTAINER
 
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Drug Details

Drug Name: OSMITROL 15% IN WATER IN PLASTIC CONTAINER
FDA Application No: (NDA) 013684
Active Ingredient(s): MANNITOL
Company: BAXTER HLTHCARE
Original Approval or Tentative Approval Date: June 8, 1964
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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
OSMITROL 10% IN WATER MANNITOL10GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 10% IN WATER IN PLASTIC CONTAINER MANNITOL10GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 15% IN WATER MANNITOL15GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 15% IN WATER IN PLASTIC CONTAINER MANNITOL15GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 20% IN WATER MANNITOL20GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 20% IN WATER IN PLASTIC CONTAINER MANNITOL20GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 5% IN WATER MANNITOL5GM/100MLINJECTABLE; INJECTION Prescription No AP
OSMITROL 5% IN WATER IN PLASTIC CONTAINER MANNITOL5GM/100MLINJECTABLE; INJECTION Prescription No AP


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