Fexofenadine
Overview
Fexofenadine is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL914).
API suppliers (15)
Suppliers of Fexofenadine evidenced by a US FDA Type II Drug Master File or an EU Certificate of Suitability (CEP). Sources: FDA DMF list, EDQM certification database.
Country recorded for 14 of 15 suppliers.
8 of 15 hold a GMP certificate on record in the EU or UK registers
- Dipharma Francis SrlItaly2 active DMF GMP on record
- MATRIX PHARMACORP PRIVATE LTDIndia1 active DMF
- VIRUPAKSHA ORGANICS LTDIndia1 active DMF
- SYNTHIMED LABS PRIVATE LIMITEDIndia1 active DMF GMP on record
- APITORIA PHARMA PRIVATE LTDIndia1 active DMF GMP on record
- VASUDHA PHARMA CHEM LTDIndia1 active DMF
- MOREPEN LABORATORIES LTDIndia1 active DMF GMP on record
- THINQ PHARMA-CRO LTDIndia1 active DMF
- CHEMECA DRUGS PRIVATE LTDIndia1 active DMF
- DR REDDYS LABORATORIES LTD1 active DMF GMP on record
- Granules India LimitedIndia1 active DMF GMP on record
- RA CHEM PHARMA LTDIndia
- Cipla USA, Inc.USA
- Sanofi-aventis Deutschland GmbhGermany GMP on record
- Sun Pharmaceutical Industries LimitedIndia GMP on record
Patent & exclusivity (US)
Per the FDA Orange Book (40 approved US products), the latest listed US patent on Fexofenadine expires 2 Aug 2030. Generic API sourcing typically opens up once these lapse.
Chemical identity
- IUPAC name
- 2-[4-[1-hydroxy-4-[4-[hydroxy(diphenyl)methyl]piperidin-1-yl]butyl]phenyl]-2-methylpropanoic acid
- Canonical SMILES
- CC(C)(C1=CC=C(C=C1)C(CCCN2CCC(CC2)C(C3=CC=CC=C3)(C4=CC=CC=C4)O)O)C(=O)O
- InChIKey
- RWTNPBWLLIMQHL-UHFFFAOYSA-N
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