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Labetalol
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Labetalol reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Labetalol-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Labetalol Hydrochloride
Labetalol EP Impurity A Hydrochloride
Labetalol EP Impurity B
Labetalol EP Impurity B Hydrochloride
Labetalol Impurity C
Labetalol EP Impurity C
Labetalol Impurity D
Labetalol EP Impurity D
Labetalol EP Impurity E
Labetalol EP Impurity F
Labetalol EP Impurity G
Labetalol RS-SR Diastereoisomer
Labetalol RR-SS Diastereoisomer
5-Bromoacetyl salicylamide
3-Amino-1-phenylbutane
5-Chloroacetylsalicylamide
5,5-Dibromoacetyl salicylamide
5-Acetyl Salicylamide
Labetalol 2-Hydroxy Impurity
Labetalol Cyclohexyl Derivative
Labetalol Impurity 1
Labetalol Impurity 2
Labetalol Impurity 3
Rac 4-(3-Aminobutyl)Phenol
N-Nitroso Labetolol
Labetalol
