NDC 66116-428
Alendronate Sodium 70 mg tablet
On the label: MedVantx, Inc.. 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 (it lists 1 site that repackages it). 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 MedVantx, Inc. 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
66116-428-04- Official label
- DailyMed (National Library of Medicine), updated Jul 1, 2013
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