NDC 70518-1192
Alendronate Sodium 35 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 35 mg
- Approval
- ANDA ANDA076768
- On the market since
- May 16, 2018
- Package NDCs
70518-1192-070518-1192-1- Official label
- DailyMed (National Library of Medicine), updated Jul 3, 2026
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