FOSAMAX
NDC 78206-135, alendronate sodium, tablet, from Organon LLC.
- Product NDC
- 78206-135
- Status
- Listed
- Labeler
- Organon LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA020560
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/78206-135 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALENDRONATE SODIUM70 mg/1
Pharmacologic classes
Bisphosphonate [EPC]; Diphosphonates [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 78206-135-01 | 78206013501 | 4 TABLET in 1 BLISTER PACK (78206-135-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/14e931fd-2c5f-4d90-b7db-5980706f4a56NADAC price for package 78206013501
GET /v1/drugs/nadac/78206013501
Use it
Look up 78206-135 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/78206-135 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 78206-135. 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.