Nauzene - 52389-612-18 - (Bryonia alba root, sepia)

Alphabetical Index


Drug Information of Nauzene

Product NDC: 52389-612
Proprietary Name: Nauzene
Non Proprietary Name: Bryonia alba root, sepia
Active Ingredient(s): 3; 12    [hp_X]/1; [hp_X]/1 & nbsp;   Bryonia alba root, sepia
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Nauzene

Product NDC: 52389-612
Labeler Name: Alva-Amco Pharmacal Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110915

Package Information of Nauzene

Package NDC: 52389-612-18
Package Description: 1 BLISTER PACK in 1 CARTON (52389-612-18) > 18 TABLET, COATED in 1 BLISTER PACK

NDC Information of Nauzene

NDC Code 52389-612-18
Proprietary Name Nauzene
Package Description 1 BLISTER PACK in 1 CARTON (52389-612-18) > 18 TABLET, COATED in 1 BLISTER PACK
Product NDC 52389-612
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bryonia alba root, sepia
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20110915
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Alva-Amco Pharmacal Companies, Inc.
Substance Name BRYONIA ALBA ROOT; SEPIA OFFICINALIS JUICE
Strength Number 3; 12
Strength Unit [hp_X]/1; [hp_X]/1
Pharmaceutical Classes

Complete Information of Nauzene


General Information