Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Gaba NDC 43742-1372
.gamma.-aminobutyric acid 8 [hp_X]/mL · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-1372-1 | 43742137201 | 30 mL in 1 BOTTLE, DROPPER (43742-1372-1)Marketed from Aug 23, 2018 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Gaba
- Generic name (nonproprietary)
- gaba
- Active ingredients
- .gamma.-aminobutyric acid — 8 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Identifiers
- Product ID 43742-1372_c50a8931-a532-4abf-890a-4e907aa6eaa5SPL ID c50a8931-a532-4abf-890a-4e907aa6eaa5SPL set ID e48e1672-4ccd-4f95-9fac-f3114e968e77UNII 2ACZ6IPC6IUPC 0810151880167
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N443742137201followed by a unit qualifier and the quantityPackage 43742-1372-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
USES: • For the temporary relief of symptoms including: • anger • hostility • sleep problems • fatigue These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.