NDC 68258-6047
Labetalol Hydrochloride 200 mg tablet, film coated
On the label: Dispensing Solutions Inc.. It's repackaged from NDC 0172-4365, made by Teva Pharmaceuticals USA, Inc. (Labetalol Hydrochloride). 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 and relabels 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 Dispensing Solutions Inc. names for other drugs.
Product details
- Generic drug
- Labetalol: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg
- Approval
- ANDA ANDA074787
- On the market since
- Jan 1, 2011
- Package NDCs
68258-6047-368258-6047-9- Official label
- DailyMed (National Library of Medicine), updated Nov 7, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?