Dextrose - 0409-4902-34 - (DEXTROSE MONOHYDRATE)

Alphabetical Index


Drug Information of Dextrose

Product NDC: 0409-4902
Proprietary Name: Dextrose
Non Proprietary Name: DEXTROSE MONOHYDRATE
Active Ingredient(s): 25    g/50mL & nbsp;   DEXTROSE MONOHYDRATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextrose

Product NDC: 0409-4902
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019445
Marketing Category: NDA
Start Marketing Date: 20110629

Package Information of Dextrose

Package NDC: 0409-4902-34
Package Description: 10 CARTON in 1 CONTAINER (0409-4902-34) > 1 SYRINGE in 1 CARTON > 50 mL in 1 SYRINGE

NDC Information of Dextrose

NDC Code 0409-4902-34
Proprietary Name Dextrose
Package Description 10 CARTON in 1 CONTAINER (0409-4902-34) > 1 SYRINGE in 1 CARTON > 50 mL in 1 SYRINGE
Product NDC 0409-4902
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110629
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE
Strength Number 25
Strength Unit g/50mL
Pharmaceutical Classes

Complete Information of Dextrose


General Information