NDC 50090-4917
Labetalol Hydrochloride 300 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged from NDC 71930-037, made by Eywa Pharma 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 A-S Medication Solutions names for other drugs.
Product details
- Generic drug
- Labetalol: every company that makes it
- Form
- tablet, film coated
- Strength
- 300 mg
- Approval
- ANDA ANDA207863
- On the market since
- May 24, 2019
- Package NDCs
50090-4917-1- Official label
- DailyMed (National Library of Medicine), updated Jun 14, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?