Albendazole
NDC 46708-681, Albendazole, tablet, film coated, from Alembic Pharmaceuticals Limited.
- Product NDC
- 46708-681
- Status
- Listed
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA215652
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/46708-681 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALBENDAZOLE200 mg/1
Pharmacologic classes
Anthelmintic [EPC]; Cytochrome P450 1A Inducers [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 46708-681-02 | 46708068102 | 2 TABLET, FILM COATED in 1 BOTTLE (46708-681-02) |
| 46708-681-28 | 46708068128 | 28 TABLET, FILM COATED in 1 BOTTLE (46708-681-28) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3b4945c7-56e9-47ed-a7ac-5078a1a50b85
Use it
Look up 46708-681 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/46708-681 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 46708-681. 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.