Alendronate Sodium
NDC 0054-0282, Alendronate Sodium, solution, from Hikma Pharmaceuticals USA Inc..
- Product NDC
- 0054-0282
- Status
- Listed
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090520
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0282 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALENDRONATE SODIUM70 mg/75mL
Pharmacologic classes
Bisphosphonate [EPC]; Diphosphonates [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0054-0282-59 | 00054028259 | 4 BOTTLE, UNIT-DOSE in 1 CARTON (0054-0282-59) / 75 mL in 1 BOTTLE, UNIT-DOSE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c910bb05-279b-4ffa-a867-46f4a0853ed5NADAC price for package 00054028259
GET /v1/drugs/nadac/00054028259
Use it
Look up 0054-0282 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0054-0282 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0054-0282. 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.