NDC 68001-382
Labetalol Hydrochloride 200 mg tablet, film coated
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Product details
- Generic drug
- Labetalol: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA207743
- On the market since
- Feb 18, 2019
- Package NDCs
68001-382-0068001-382-03- Official label
- DailyMed (National Library of Medicine), updated Jun 8, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?