Dextrose - 0338-0711-34 - (Dextrose Monohydrate)

Alphabetical Index


Drug Information of Dextrose

Product NDC: 0338-0711
Proprietary Name: Dextrose
Non Proprietary Name: Dextrose Monohydrate
Active Ingredient(s): 20    g/100mL & nbsp;   Dextrose Monohydrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextrose

Product NDC: 0338-0711
Labeler Name: Baxter Healthcare Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017521
Marketing Category: NDA
Start Marketing Date: 19790828

Package Information of Dextrose

Package NDC: 0338-0711-34
Package Description: 1000 mL in 1 BAG (0338-0711-34)

NDC Information of Dextrose

NDC Code 0338-0711-34
Proprietary Name Dextrose
Package Description 1000 mL in 1 BAG (0338-0711-34)
Product NDC 0338-0711
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextrose Monohydrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19790828
Marketing Category Name NDA
Labeler Name Baxter Healthcare Company
Substance Name DEXTROSE MONOHYDRATE
Strength Number 20
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Dextrose


General Information