01 1Cadila Healthcare Limited
02 1Hetero Labs Limited
03 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
04 1Syn-Tech Chem. & Pharm. Co. , Ltd.
05 1Tateyama Chemical Co., Ltd.
06 1Tianish Laboratories Private Limited
01 2Atomoxetine Hydrochloride
02 2Atomoxetine hydrochloride
03 1Atomoxetine hydrochloride
04 1Atomoxetine hydrochloride "Tateyama"
01 2India
02 1Italy
03 1Japan
04 1Taiwan
05 1U.S.A
Registration Number : 229MF10156
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2017-08-08
Latest Date of Registration : 2017-08-08
Atomoxetine hydrochloride (Teva)
Registration Number : 306MF10005
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2024-01-11
Latest Date of Registration : 2024-01-11
Registration Number : 229MF10113
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2017-06-30
Latest Date of Registration : 2017-06-30
Atomoxetine hydrochloride "Tateyama"
Registration Number : 229MF10133
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2017-07-19
Latest Date of Registration : 2023-02-02
Registration Number : 229MF10128
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
Registration Number : 303MF10088
Registrant's Address : Zydus Corporate Park, 3rd Floor, B Wing, Scheme No. 63, Survey No. 536, Plot No. 103,...
Initial Date of Registration : 2021-06-07
Latest Date of Registration : 2021-06-07
A Atomoxetin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atomoxetin Hydrochloride, including repackagers and relabelers. The FDA regulates Atomoxetin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atomoxetin Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Atomoxetin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atomoxetin Hydrochloride supplier is an individual or a company that provides Atomoxetin Hydrochloride active pharmaceutical ingredient (API) or Atomoxetin Hydrochloride finished formulations upon request. The Atomoxetin Hydrochloride suppliers may include Atomoxetin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Atomoxetin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Atomoxetin Hydrochloride Drug Master File in Japan (Atomoxetin Hydrochloride JDMF) empowers Atomoxetin Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Atomoxetin Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Atomoxetin Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Atomoxetin Hydrochloride suppliers with JDMF on PharmaCompass.
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