Amantadine
NDC 46708-586, Amantadine, tablet, from Alembic Pharmaceuticals Limited.
- Product NDC
- 46708-586
- Status
- Listed
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA214284
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/46708-586 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AMANTADINE HYDROCHLORIDE100 mg/1
Pharmacologic classes
Influenza A M2 Protein Inhibitor [EPC]; M2 Protein Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 46708-586-31 | 46708058631 | 100 TABLET in 1 BOTTLE (46708-586-31) |
| 46708-586-71 | 46708058671 | 500 TABLET in 1 BOTTLE (46708-586-71) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/48fa07c8-8b95-40d7-a0f5-132577dfb2c8
Use it
Look up 46708-586 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/46708-586 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 46708-586. 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.