Gaba - 43857-0123-1 - (Gaba)

Alphabetical Index


Drug Information of Gaba

Product NDC: 43857-0123
Proprietary Name: Gaba
Non Proprietary Name: Gaba
Active Ingredient(s): 6    [hp_X]/mL & nbsp;   Gaba
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Gaba

Product NDC: 43857-0123
Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20130108

Package Information of Gaba

Package NDC: 43857-0123-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (43857-0123-1)

NDC Information of Gaba

NDC Code 43857-0123-1
Proprietary Name Gaba
Package Description 30 mL in 1 BOTTLE, DROPPER (43857-0123-1)
Product NDC 43857-0123
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Gaba
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20130108
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name BioActive Nutritional, Inc.
Substance Name .GAMMA.-AMINOBUTYRIC ACID
Strength Number 6
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Gaba


General Information