NDC 71205-714
Risedronate Sodium 35 mg tablet, film coated
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Apotex Corp.'s NDC 60505-3165.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apotex Inc. | Toronto, Canada | Makes it and tests it | No problems foundSep 25, 2026 · 11 inspections, 2 with FDA action |
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · relabels it
Product details
- Generic drug
- Risedronic Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 35 mg
- Approval
- ANDA ANDA090877
- On the market since
- Nov 30, 2015
- Package NDCs
71205-714-04- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2022
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