NDC 50090-4076
Alendronate Sodium 35 mg tablet
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Cipla USA., Inc.'s NDC 69097-223.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cipla Limited | Salcette, India | Makes it | Problems found, fixed voluntarilyJun 21, 2024 · 12 inspections, 2 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet
- Strength
- 35 mg
- Approval
- ANDA ANDA076768
- On the market since
- Aug 4, 2008
- Package NDCs
50090-4076-0- Official label
- DailyMed (National Library of Medicine), updated Apr 16, 2021
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