NDC 70771-1164-5
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 Zydus Lifesciences Limited.
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
70771-1164-5- NDC Code (Product)
70771-1164- Manufacturer
- Zydus Lifesciences Limited
- Strength
- 200 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.