NDC 68258-3014
Alendronate Sodium 70 mg tablet
On the label: Dispensing Solutions Inc.. It's repackaged from NDC 16262-601, which isn't on any FDA listing we can find.
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 Dispensing Solutions Inc. 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
- Mar 3, 2009
- Package NDCs
16262-601-4468258-3014-1- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?