NDC 68071-3878
Labetalol Hydrochloride 200 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Biocon Pharma Inc.'s NDC 70377-061.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
| Piramal Pharma Limited | Pithampur, India | Makes it, tests it and packages it | No problems foundMay 19, 2023 · 8 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Labetalol: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA209603
- On the market since
- May 27, 2021
- Package NDCs
68071-3878-9- Official label
- DailyMed (National Library of Medicine), updated Jul 28, 2025
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