Atomoxetine Hydrochloride

Overview

Atomoxetine Hydrochloride is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL1702).

API suppliers (7)

Suppliers of Atomoxetine Hydrochloride evidenced by a US FDA Type II Drug Master File or an EU Certificate of Suitability (CEP). Sources: FDA DMF list, EDQM certification database.

• TAPI NL BVNetherlands1 active DMF
• SCI PHARMTECH INCTaiwan1 active DMF
• Shandong Loncom Pharmaceutical Co.,ltd.China1 active DMF
• Hetero Labs LimitedIndia1 active DMF GMP on record
• Macleods Pharmaceuticals Ltd.India1 active DMF GMP on record
• Zhejiang Jiuzhou Pharmaceutical Co., Ltd.China GMP on record
• Zydus Lifesciences LimitedIndiaCEP GMP on record

EU CEP holders (6)

Companies holding a valid EU Certificate of Suitability (CEP) for Atomoxetine Hydrochloride, from the EDQM certification database. A CEP holder is a documented EU-market source of the substance — not necessarily the manufacturer — and these are not yet profiled in our directory.

Chemical identity

IUPAC name

(3R)-N-methyl-3-(2-methylphenoxy)-3-phenylpropan-1-amine;hydrochloride

Canonical SMILES

CC1=CC=CC=C1O[C@H](CCNC)C2=CC=CC=C2.Cl

InChIKey

LUCXVPAZUDVVBT-UNTBIKODSA-N