VIGABATRIN
NDC 69097-964, vigabatrin, powder, for solution, from Cipla USA, Inc..
- Product NDC
- 69097-964
- Status
- Listed
- Labeler
- Cipla USA, Inc.
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA211592
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69097-964 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- VIGABATRIN500 mg/mL
Pharmacologic classes
Anti-epileptic Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69097-964-53 | 69097096453 | 50 PACKET in 1 CARTON (69097-964-53) / 10 mL in 1 PACKET |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/823cc915-0350-4780-85ed-cd1c338e429d
Use it
Look up 69097-964 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69097-964 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69097-964. 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.