Dextrose - 0409-7100-67 - (DEXTROSE MONOHYDRATE)

Alphabetical Index


Drug Information of Dextrose

Product NDC: 0409-7100
Proprietary Name: Dextrose
Non Proprietary Name: DEXTROSE MONOHYDRATE
Active Ingredient(s): 50    mg/mL & nbsp;   DEXTROSE MONOHYDRATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextrose

Product NDC: 0409-7100
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA019466
Marketing Category: ANDA
Start Marketing Date: 20101101

Package Information of Dextrose

Package NDC: 0409-7100-67
Package Description: 10 CONTAINER in 1 CASE (0409-7100-67) > 5 BAG in 1 CONTAINER > 100 mL in 1 BAG

NDC Information of Dextrose

NDC Code 0409-7100-67
Proprietary Name Dextrose
Package Description 10 CONTAINER in 1 CASE (0409-7100-67) > 5 BAG in 1 CONTAINER > 100 mL in 1 BAG
Product NDC 0409-7100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20101101
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DEXTROSE MONOHYDRATE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Dextrose


General Information