A    B    C    D    E    F    G    H    I    J    K    L    M    N    O    P    Q    R    S    T    U    V    W    X    Y    Z    
Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Levocabastine, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Levocabastine impurity reference standards are invaluable for pharmaceutical research, supporting product development, ANDA and DMF submissions, quality control (QC), method validation, and stability studies. They also aid in identifying unknown impurities and assessing genotoxic potential.
Our Levocabastine-related products undergo thorough characterization and are supplied with detailed Certificates of Analysis (COA) and analytical data that meet regulatory requirements. All supplied products are re-tested at regular intervals to ensure ongoing quality and compliance.

Levocabastine Related Compounds

Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Levocabastine Hydrochloride EP Impurity D Impurity CS-EO-03650 80139-90-8 Enquire
Levocabastine Impurity 2 Impurity CS-O-58140 83863-68-7 Enquire
Ethoxy levocabastine Impurity CS-O-37526 Not Available Enquire
Ethyl ester of levocabastine Impurity CS-O-37527 Not Available Enquire
levocabastine hydrochloride impurity A Impurity CS-O-37521 Not Available Enquire
levocabastine hydrochloride impurity B Impurity CS-O-37523 Not Available Enquire
levocabastine hydrochloride impurity E Impurity CS-O-37524 Not Available Enquire


Nitrosamine

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Levocabastine Nitroso impurity Nitrosamine CS-O-60548 ---- Enquire