GABA
- Product NDC
- 43742-1372
- 11-digit product format
- 437421372
- Labeler code
- 43742
- Product ID
- 43742-1372_c50a8931-a532-4abf-890a-4e907aa6eaa5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GABA
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-08-23
- Substance
- .GAMMA.-AMINOBUTYRIC ACID
- Active strength
- 8 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- GABA
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| .GAMMA.-AMINOBUTYRIC ACID | 8 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2ACZ6IPC6I |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43742-1372-1 | GABA | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43742-1372 | GABA LIQUID [DESERET BIOLOGICALS, INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240308_e48e1672-4ccd-4f95-9fac-f3114e968e77.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1372-1 | 43742137201 | 30 mL in 1 BOTTLE, DROPPER (43742-1372-1) | 30 ml | 2018-08-23 | 0000-00-00 | No | No | Current |