Dextrose - 54868-3089-1 - (Dextrose)

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Drug Information of Dextrose

Product NDC: 54868-3089
Proprietary Name: Dextrose
Non Proprietary Name: Dextrose
Active Ingredient(s): 25    g/50mL & nbsp;   Dextrose
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextrose

Product NDC: 54868-3089
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019445
Marketing Category: NDA
Start Marketing Date: 20061211

Package Information of Dextrose

Package NDC: 54868-3089-1
Package Description: 25 VIAL in 1 TRAY (54868-3089-1) > 50 mL in 1 VIAL

NDC Information of Dextrose

NDC Code 54868-3089-1
Proprietary Name Dextrose
Package Description 25 VIAL in 1 TRAY (54868-3089-1) > 50 mL in 1 VIAL
Product NDC 54868-3089
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextrose
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20061211
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name DEXTROSE MONOHYDRATE
Strength Number 25
Strength Unit g/50mL
Pharmaceutical Classes

Complete Information of Dextrose


General Information