Nauzene - 52389-142-40 - (Glucose, Fructose, Sodium Citrate)

Alphabetical Index


Drug Information of Nauzene

Product NDC: 52389-142
Proprietary Name: Nauzene
Non Proprietary Name: Glucose, Fructose, Sodium Citrate
Active Ingredient(s): 968; 175; 230    mg/1; mg/1; mg/1 & nbsp;   Glucose, Fructose, Sodium Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Nauzene

Product NDC: 52389-142
Labeler Name: Alva-Amco Pharmacal Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part357
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20000708

Package Information of Nauzene

Package NDC: 52389-142-40
Package Description: 4 BLISTER PACK in 1 CARTON (52389-142-40) > 10 TABLET, CHEWABLE in 1 BLISTER PACK

NDC Information of Nauzene

NDC Code 52389-142-40
Proprietary Name Nauzene
Package Description 4 BLISTER PACK in 1 CARTON (52389-142-40) > 10 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC 52389-142
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Glucose, Fructose, Sodium Citrate
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20000708
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Alva-Amco Pharmacal Companies, Inc.
Substance Name DEXTROSE; FRUCTOSE; TRISODIUM CITRATE DIHYDRATE
Strength Number 968; 175; 230
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Nauzene


General Information