NDC 0054-0282
Alendronate Sodium 70 mg per 75 mL solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Recalls
- Apr 7, 2026 · Class II · Hikma Pharmaceuticals USA INC
This recall is being conducted due to out of specification assay results in a limited number of bottles that were stored on side.
Lots: Lot # AC2040A, Exp Date: 04/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- solution, oral
- Strength
- 70 mg per 75 mL
- Approval
- ANDA ANDA090520
- On the market since
- Oct 30, 2020
- Package NDCs
0054-0282-59- Official label
- DailyMed (National Library of Medicine), updated Jan 15, 2026
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