United States · FDA National Drug Code directory
GABA
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 43742-1372_c50a8931-a532-4abf-890a-4e907aa6eaa5
- Product NDC
- 43742-1372
- Form
- LIQUID
- Composition / generic term
- GABA
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 20180823
- Source listing expiry
- 20261231
Source-listed ingredients
- .GAMMA.-AMINOBUTYRIC ACID — 8 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 mL in 1 BOTTLE, DROPPER (43742-1372-1) · 43742-1372-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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