NDC 43742-0695

GABA

Gaba

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

• Product ID: 43742-0695_2839ed69-cb05-4298-8e3e-5fe5f2177142
• NDC: 43742-0695
• Product Type: Human Otc Drug
• Proprietary Name: GABA
• Generic Name: Gaba
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2015-12-09
• Marketing End Date: 2023-07-23
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Deseret Biologicals, Inc.
• Substance Name: .GAMMA.-AMINOBUTYRIC ACID
• Active Ingredient Strength: 6 [hp_X]/mL
• NDC Exclude Flag: N

Packaging

NDC 43742-0695-1

30 mL in 1 BOTTLE, DROPPER (43742-0695-1)

• Marketing Start Date: 2015-12-09
• Marketing End Date: 2023-07-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 43742-0695-1 [43742069501]

GABA LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2015-12-09
• Marketing End Date: 2023-07-23

Drug Details

Active Ingredients

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

OpenFDA Data

• SPL SET ID: 04e3aa4c-73dc-4e89-8736-d3443d2df9a5
• Manufacturer:
  • Deseret Biologicals, Inc.
• UNII:
  • 2ACZ6IPC6I

NDC Crossover Matching brand name "GABA" or generic name "Gaba"

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