NDC 68071-3340
Alendronate Sodium 70 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
- NuCare Pharmaceuticals,Inc., Orange, 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
- Aug 4, 2008
- Package NDCs
68071-3340-4- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2026
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