NDC 33261-820
Alendronate Sodium 70 mg tablet
On the label: Aidarex Pharmaceuticals LLC. It's repackaged from NDC 0093-5171, made by Teva Pharmaceuticals USA, Inc. (Alendronate Sodium). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Aidarex Pharmaceuticals LLC names for other drugs.
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet
- Strength
- 70 mg
- Approval
- ANDA ANDA075710
- On the market since
- Feb 6, 2008
- Package NDCs
33261-820-01- Official label
- DailyMed (National Library of Medicine), updated Jun 21, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?