NDC 68382-800-01
Labetalol Hydrochloride 300 mg/1
Labetalol Hydrochloride · TABLET, FILM COATED
Labetalol Hydrochloride is a tablet, film coated containing labetalol hydrochloride at a strength of 300 mg/1. Manufactured by Zydus Pharmaceuticals USA Inc..
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
68382-800-01- NDC Code (Product)
68382-800- Manufacturer
- Zydus Pharmaceuticals USA Inc.
- Strength
- 300 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA207743
- Marketing Start
- 12/05/2017
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.