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Gaba
Gaba - 43857-0123-1 - (Gaba)
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 |
