NDC 68788-7130
Alendronate Sodium 70 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Cipla USA., Inc.'s NDC 69097-224.
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
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · relabels it
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 70 mg
- Approval
- ANDA ANDA076768
- On the market since
- Mar 30, 2018
- Package NDCs
68788-7130-4- Official label
- DailyMed (National Library of Medicine), updated Feb 16, 2026
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