Strength
200 mg/1
Manufacturer
Eywa Pharma IncNDC
71930003652
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LABETALOL HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA207863On Market Since
5/24/2019
Pharmacological Classes
Adrenergic beta-Antagonists
beta-Adrenergic Blocker
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