NDC 55154-2143
Labetalol Hydrochloride 200 mg tablet, film coated
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from BluePoint Laboratories.'s NDC 68001-382.
Where the pills inside were 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
- Dec 10, 2024
- Package NDCs
55154-2143-0- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2026
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