ALENDRONATE SODIUM
NDC 50090-4692, Alendronate sodium, tablet, from A-S Medication Solutions.
- Product NDC
- 50090-4692
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076768
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-4692 \ -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 |
|---|---|---|
| 50090-4692-0 | 50090469200 | 1 BLISTER PACK in 1 CARTON (50090-4692-0) / 4 TABLET in 1 BLISTER PACK |
| 50090-4692-1 | 50090469201 | 3 BLISTER PACK in 1 CARTON (50090-4692-1) / 4 TABLET in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/fe1dd324-eb02-4a73-97f5-9b77a7df10a7
Use it
Look up 50090-4692 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-4692 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-4692. 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.