NDC 71205-048
Alendronate Sodium 70 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Aurobindo Pharma Limited's NDC 65862-329.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · relabels it
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 70 mg
- Approval
- ANDA ANDA090124
- On the market since
- Aug 4, 2008
- Package NDCs
71205-048-04- Official label
- DailyMed (National Library of Medicine), updated Mar 1, 2023
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