Gabapentin
NDC 72162-2142, GABAPENTIN, tablet, film coated, from Bryant Ranch Prepack.
- Product NDC
- 72162-2142
- Status
- Listed
- Labeler
- Bryant Ranch Prepack
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203244
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2142 \ -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 |
|---|---|---|
| 72162-2142-1 | 72162214201 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2142-1) |
| 72162-2142-5 | 72162214205 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2142-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/56967a93-b3c0-4043-9241-585fc64e2624
Use it
Look up 72162-2142 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2142 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72162-2142. 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.