NDC 67046-1697
Labetalol Hydrochloride 200 mg tablet
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from BluePoint Laboratories.'s NDC 68001-701.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Labetalol: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA074787
- On the market since
- Oct 19, 2026
- Package NDCs
67046-1697-3- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2026
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