NDC 61919-729
Alendronate Sodium 35 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx 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
- Direct Rx, Dawsonville, GA, United States · repackages it
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet
- Strength
- 35 mg
- Approval
- ANDA ANDA076768
- On the market since
- Jan 18, 2019
- Package NDCs
61919-729-04- Official label
- DailyMed (National Library of Medicine), updated Jan 18, 2019
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