NDC 55154-0182-0
Labetalol Hydrochloride 200 mg/1
Labetalol Hydrochloride · TABLET, FILM COATED
Labetalol Hydrochloride is a tablet, film coated containing labetalol hydrochloride at a strength of 200 mg/1. Manufactured by Cardinal Health 107, LLC.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
55154-0182-0- NDC Code (Product)
55154-0182- Manufacturer
- Cardinal Health 107, LLC
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA209603
- Marketing Start
- 05/06/2025
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.