NDC 50090-7731-0
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 A-S Medication Solutions.
Key Facts
- Brand Name
- LABETALOL HYDROCHLORIDE
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
50090-7731-0- NDC Code (Product)
50090-7731- Manufacturer
- A-S Medication Solutions
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA211953
- Marketing Start
- 08/18/2021
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.