NDC 70518-4201-0
Labetalol Hydrochloride 100 mg/1
Labetalol Hydrochloride · TABLET, FILM COATED
Labetalol Hydrochloride is a tablet, film coated containing labetalol hydrochloride at a strength of 100 mg/1. Manufactured by REMEDYREPACK INC..
Key Facts
- Brand Name
- Labetalol Hydrochloride
- Generic Name
- Labetalol Hydrochloride
- NDC Code (Package)
70518-4201-0- NDC Code (Product)
70518-4201- Manufacturer
- REMEDYREPACK INC.
- Strength
- 100 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA075215
- Drug Class
- beta-Adrenergic Blocker [EPC]
- Marketing Start
- 10/02/2024
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.