DEXTROSE - 0338-0017-41 - (DEXTROSE MONOHYDRATE)

Alphabetical Index


Drug Information of DEXTROSE

Product NDC: 0338-0017
Proprietary Name: DEXTROSE
Non Proprietary Name: DEXTROSE MONOHYDRATE
Active Ingredient(s): 50    g/1000mL & nbsp;   DEXTROSE MONOHYDRATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of DEXTROSE

Product NDC: 0338-0017
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA016673
Marketing Category: ANDA
Start Marketing Date: 20100616

Package Information of DEXTROSE

Package NDC: 0338-0017-41
Package Description: 1 BAG in 1 PACKAGE (0338-0017-41) > 50 mL in 1 BAG

NDC Information of DEXTROSE

NDC Code 0338-0017-41
Proprietary Name DEXTROSE
Package Description 1 BAG in 1 PACKAGE (0338-0017-41) > 50 mL in 1 BAG
Product NDC 0338-0017
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXTROSE MONOHYDRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20100616
Marketing Category Name ANDA
Labeler Name Baxter Healthcare Corporation
Substance Name DEXTROSE MONOHYDRATE
Strength Number 50
Strength Unit g/1000mL
Pharmaceutical Classes

Complete Information of DEXTROSE


General Information