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Clearsynth is a leading innovator in pharmaceutical reference standards, offering high-quality Reference Standards for Fexofenadine Hydrochloride, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Our Fexofenadine Hydrochloride 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 Fexofenadine Hydrochloride-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.

Fexofenadine Hydrochloride Related Compounds

Stable Isotopes

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fexofenadine hydrochloride 13C12 Stable Isotopes CS-EK-02927 153439-40-8 unlabeled Enquire


API

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fexofenadine Hydrochloride API CS-O-00610 153439-40-8 In Stock


Impurity

COMPOUND CATEGORY CAT. No. CAS. No. STOCK STATUS
Fexofenadine Hydrochloride EP Impurity D Impurity CS-T-54705 154825-96-4 In Stock
Fexofenadine Hydrochloride EP Impurity F Impurity CS-O-14191 185066-33-5 Enquire
Fexofenadine hydrochloride USP Impurity A Impurity CS-EN-00073 Not Available Enquire
meta-Fexofenadine Hydrochloride Impurity CS-T-93671 479035-75-1 (Free Base) Enquire