Glutose - 0574-0069-15 - (dextrose)

Alphabetical Index


Drug Information of Glutose

Product NDC: 0574-0069
Proprietary Name: Glutose
Non Proprietary Name: dextrose
Active Ingredient(s): 15    g/37.5g & nbsp;   dextrose
Administration Route(s): ORAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Glutose

Product NDC: 0574-0069
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED OTHER
Start Marketing Date: 19960201

Package Information of Glutose

Package NDC: 0574-0069-15
Package Description: 37.5 g in 1 TUBE (0574-0069-15)

NDC Information of Glutose

NDC Code 0574-0069-15
Proprietary Name Glutose
Package Description 37.5 g in 1 TUBE (0574-0069-15)
Product NDC 0574-0069
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextrose
Dosage Form Name GEL
Route Name ORAL
Start Marketing Date 19960201
Marketing Category Name UNAPPROVED OTHER
Labeler Name Paddock Laboratories, Inc.
Substance Name DEXTROSE
Strength Number 15
Strength Unit g/37.5g
Pharmaceutical Classes

Complete Information of Glutose


General Information