NDC 60723-207
Alendronate 35 mg tablet
On the label: Hangzhou Minsheng Binjiang Pharmaceutical CO., Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hangzhou Minsheng Binjiang Pharmaceutical Co.,Ltd | Hangzhou, China | Makes it | Serious problems, FDA actionMar 7, 2025 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 35 mg
- Approval
- ANDA ANDA090258
- On the market since
- Dec 5, 2017
- Package NDCs
60723-207-3160723-207-3260723-207-33- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2025
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