GABAPENTIN
NDC 85509-1166, Gabapentin, tablet, from PHOENIX RX LLC.
- Product NDC
- 85509-1166
- Status
- Listed
- Labeler
- PHOENIX RX LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214957
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1166 \ -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 |
|---|---|---|
| 85509-1166-3 | 85509116603 | 30 TABLET in 1 BOTTLE (85509-1166-3) |
| 85509-1166-6 | 85509116606 | 60 TABLET in 1 BOTTLE (85509-1166-6) |
| 85509-1166-9 | 85509116609 | 90 TABLET in 1 BOTTLE (85509-1166-9) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5a85ea98-4211-54eb-e063-6294a90aff33
Use it
Look up 85509-1166 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/85509-1166 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 85509-1166. 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.