Gabapentin
NDC 80425-0035, Gabapentin, tablet, from Advanced Rx of Tennessee, LLC.
- Product NDC
- 80425-0035
- Status
- Listed
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206402
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0035 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GABAPENTIN800 mg/1
Pharmacologic classes
Decreased Central Nervous System Disorganized Electrical Activity [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 80425-0035-1 | 80425003501 | 30 TABLET in 1 BOTTLE (80425-0035-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/afa28969-91ca-83fd-e053-2a95a90a656b
Use it
Look up 80425-0035 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0035 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80425-0035. 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.