Mannitol - 55154-3192-8 - (MANNITOL)

Alphabetical Index


Drug Information of Mannitol

Product NDC: 55154-3192
Proprietary Name: Mannitol
Non Proprietary Name: MANNITOL
Active Ingredient(s): 12.5    g/50mL & nbsp;   MANNITOL
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mannitol

Product NDC: 55154-3192
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA016269
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of Mannitol

Package NDC: 55154-3192-8
Package Description: 1 VIAL, SINGLE-DOSE in 1 BAG (55154-3192-8) > 50 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Mannitol

NDC Code 55154-3192-8
Proprietary Name Mannitol
Package Description 1 VIAL, SINGLE-DOSE in 1 BAG (55154-3192-8) > 50 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55154-3192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MANNITOL
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name MANNITOL
Strength Number 12.5
Strength Unit g/50mL
Pharmaceutical Classes Increased Diuresis [PE],Osmotic Activity [MoA],Osmotic Diuretic [EPC]

Complete Information of Mannitol


General Information