NDC 68001-700-00
Labetalol Hydrochloride 100 mg/1
Labetalol Hydrochloride · TABLET
Labetalol Hydrochloride is a tablet containing labetalol hydrochloride at a strength of 100 mg/1. Manufactured by BluePoint Laboratories.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
68001-700-00- NDC Code (Product)
68001-700- Manufacturer
- BluePoint Laboratories
- Strength
- 100 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA074787
- Marketing Start
- 03/15/2026
Recall History
No Recall HistoryView Full Drug Page
Labetalol Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.