Gabapentin
NDC 69367-346, Gabapentin, tablet, coated, from Westminster Pharmaceuticals, LLC.
- Product NDC
- 69367-346
- Status
- Listed
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207057
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69367-346 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GABAPENTIN600 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69367-346-05 | 69367034605 | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-346-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2eec52a1-9016-46dd-8b4c-8dab1d0aeeceNADAC price for package 69367034605
GET /v1/drugs/nadac/69367034605
Use it
Look up 69367-346 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69367-346 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69367-346. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.