NDC 0591-0606-01
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 Actavis Pharma, Inc..
Key Facts
- Brand Name
- Labetalol hydrochloride
- Generic Name
- Labetalol hydrochloride
- NDC Code (Package)
0591-0606-01- NDC Code (Product)
0591-0606- Manufacturer
- Actavis Pharma, Inc.
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA075133
- Marketing Start
- 08/03/1998
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.