Osmitrol - 0338-0357-02 - (Mannitol)

Alphabetical Index


Drug Information of Osmitrol

Product NDC: 0338-0357
Proprietary Name: Osmitrol
Non Proprietary Name: Mannitol
Active Ingredient(s): 20    g/100mL & nbsp;   Mannitol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Osmitrol

Product NDC: 0338-0357
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA013684
Marketing Category: NDA
Start Marketing Date: 19640608

Package Information of Osmitrol

Package NDC: 0338-0357-02
Package Description: 250 mL in 1 BAG (0338-0357-02)

NDC Information of Osmitrol

NDC Code 0338-0357-02
Proprietary Name Osmitrol
Package Description 250 mL in 1 BAG (0338-0357-02)
Product NDC 0338-0357
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mannitol
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19640608
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name MANNITOL
Strength Number 20
Strength Unit g/100mL
Pharmaceutical Classes Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]

Complete Information of Osmitrol


General Information