NDC 43857-0123

GABA

Gaba (gamma-aminobutyric Acid)

GABA is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Bioactive Nutritional, Inc.. The primary component is .gamma.-aminobutyric Acid.

• Product ID: 43857-0123_24c12661-ff0c-40a0-a64e-038e1e0a491c
• NDC: 43857-0123
• Product Type: Human Otc Drug
• Proprietary Name: GABA
• Generic Name: Gaba (gamma-aminobutyric Acid)
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2014-10-03
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: BioActive Nutritional, Inc.
• Substance Name: .GAMMA.-AMINOBUTYRIC ACID
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 43857-0123-1

30 mL in 1 BOTTLE, DROPPER (43857-0123-1)

• Marketing Start Date: 2016-08-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43857-0123-1 [43857012301]

GABA LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2016-08-16

Drug Details

Active Ingredients

Ingredient	Strength
.GAMMA.-AMINOBUTYRIC ACID	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 4fe29a89-c4d6-446c-b5f7-692762c58614
• Manufacturer:
  • BioActive Nutritional, Inc.
• UNII:
  • 2ACZ6IPC6I

NDC Crossover Matching brand name "GABA" or generic name "Gaba (gamma-aminobutyric Acid)"

NDC	Brand Name	Generic Name
43742-0178	GABA	GABA,
43742-0695	GABA	GABA
43742-1372	GABA	GABA
43857-0123	GABA	Gaba (Gamma-Aminobutyric Acid)
43857-0149	Gaba	Gaba
63083-1519	GABA	GABA
63776-690	GABA	Gamma.-Aminobutyric Acid