Mannitol - 0517-4050-25 - (mannitol)

Alphabetical Index


Drug Information of Mannitol

Product NDC: 0517-4050
Proprietary Name: Mannitol
Non Proprietary Name: mannitol
Active Ingredient(s): 250    mg/mL & nbsp;   mannitol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mannitol

Product NDC: 0517-4050
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA087409
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Mannitol

Package NDC: 0517-4050-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4050-25) > 50 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Mannitol

NDC Code 0517-4050-25
Proprietary Name Mannitol
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4050-25) > 50 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-4050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mannitol
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name American Regent, Inc.
Substance Name MANNITOL
Strength Number 250
Strength Unit mg/mL
Pharmaceutical Classes Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]

Complete Information of Mannitol


General Information