Alendronate Sodium
NDC 50090-5677, Alendronate Sodium, tablet, from A-S Medication Solutions.
- Product NDC
- 50090-5677
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090124
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-5677 \ -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 |
|---|---|---|
| 50090-5677-0 | 50090567700 | 1 BLISTER PACK in 1 CARTON (50090-5677-0) / 4 TABLET in 1 BLISTER PACK |
| 50090-5677-1 | 50090567701 | 3 BLISTER PACK in 1 CARTON (50090-5677-1) / 4 TABLET in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/eeb65442-6b3c-485c-9c5d-9cf40df4451e
Use it
Look up 50090-5677 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-5677 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-5677. 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.