NDC 55695-012
alendronate sodium 70 mg tablet
On the label: Department of State Health Services, Pharmacy Branch. It's repackaged from NDC 16252-601, made by Actavis Pharma, 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 Department of State Health Services, Pharmacy Branch names for other drugs.
Product details
- Generic drug
- Alendronic Acid: every company that makes it
- Form
- tablet
- Strength
- 70 mg
- Approval
- ANDA ANDA076984
- On the market since
- Aug 4, 2008
- Package NDCs
55695-012-00- Official label
- DailyMed (National Library of Medicine), updated Feb 9, 2016
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