Clemastine Fumarate
NDC 64950-268, Clemastine Fumarate, tablet, from Genus Lifesciences.
- Product NDC
- 64950-268
- Status
- Listed
- Labeler
- Genus Lifesciences
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA073283
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/64950-268 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CLEMASTINE FUMARATE2.68 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 64950-268-03 | 64950026803 | 30 TABLET in 1 BOTTLE (64950-268-03) |
| 64950-268-10 | 64950026810 | 100 TABLET in 1 BOTTLE (64950-268-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/cf8a3449-8bb3-4d5c-8d0d-557590e49ee5NADAC price for package 64950026810
GET /v1/drugs/nadac/64950026810
Use it
Look up 64950-268 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/64950-268 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 64950-268. 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.