01 1Active Pharma Co., Ltd.
02 1Assia Chemical Industries Ltd.
03 1Daito Co., Ltd.
04 1JUBILANT BIOSYS LIMITED.
05 1Osaka Synthetic Organic Chemistry Research Institute Co., Ltd.
06 2Shijiazhuang Lonzeal Pharmaceuticals Co. , Ltd.
07 1Sumitomo Chemical Co., Ltd.
08 1Zydus Lifesciences Limited
01 1Japanese Pharmacopoeia Paroxetine Hydrochloride Hydrate
02 1Only the Japanese Pharmacopoeia paroxetine hydrochloride hydrate production
03 1Paroxetine Hydrochloride Hydrate
04 5Paroxetine hydrochloride hydrate
05 1Paroxetine hydrochloride hydrate "Teva"
01 2China
02 2India
03 1Israel
04 4Japan
Paroxetine hydrochloride hydrate "Teva"
Registration Number : 223MF10002
Registrant's Address : Neot-Hovav Eco-Industrial Park, Be'er Sheva 8412316, Israel
Initial Date of Registration : 2011-01-07
Latest Date of Registration : 2011-11-17
Paroxetine hydrochloride hydrate
Registration Number : 222MF10257
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2010-11-18
Latest Date of Registration : 2011-11-07
Japanese Pharmacopoeia Paroxetine Hydrochloride Hydrate
Registration Number : 231MF10081
Registrant's Address : 1-A, Sector 16-A, Institutional Area, Noida 201 301, Uttar Pradesh, India
Initial Date of Registration : 2019-04-03
Latest Date of Registration : 2019-04-03
Japanese Pharmacopoeia Paroxetine Hydrochloride Hydrate (For Manufacturing Use Only)
Registration Number : 227MF10216
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2015-08-31
Latest Date of Registration : 2015-08-31
Paroxetine hydrochloride hydrate
Registration Number : 222MF10283
Registrant's Address : 2-36-1 Kanda Jimbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2010-12-27
Latest Date of Registration : 2012-10-01
Paroxetine hydrochloride hydrate
Registration Number : 307MF10061
Registrant's Address : Industrial Zone Shenze (No. 16, West Ring Road), Shijiazhuang, Hebei Province 052560 ...
Initial Date of Registration : 2025-05-14
Latest Date of Registration : 2025-05-14
Paroxetine hydrochloride hydrate
Registration Number : 304MF10042
Registrant's Address : Industrial Zone Shenze (No. 16, West Ring Road), Shijiazhuang, Hebei Province 052560 ...
Initial Date of Registration : 2022-02-24
Latest Date of Registration : 2022-02-24
Paroxetine hydrochloride hydrate
Registration Number : 222MF10199
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2010-07-14
Latest Date of Registration : 2010-07-14
Paroxetine Hydrochloride Hydrate
Registration Number : 222MF10207
Registrant's Address : Zydus Corporate Park, 3rd Floor, B Wing, Scheme No. 63, Survey No. 536, Plot No. 103,...
Initial Date of Registration : 2010-07-26
Latest Date of Registration : 2017-09-25
18
PharmaCompass offers a list of Paroxetine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier for your needs.
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A C19H20FNO3 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C19H20FNO3, including repackagers and relabelers. The FDA regulates C19H20FNO3 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C19H20FNO3 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 C19H20FNO3 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A C19H20FNO3 supplier is an individual or a company that provides C19H20FNO3 active pharmaceutical ingredient (API) or C19H20FNO3 finished formulations upon request. The C19H20FNO3 suppliers may include C19H20FNO3 API manufacturers, exporters, distributors and traders.
click here to find a list of C19H20FNO3 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 C19H20FNO3 Drug Master File in Japan (C19H20FNO3 JDMF) empowers C19H20FNO3 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 C19H20FNO3 JDMF during the approval evaluation for pharmaceutical products. At the time of C19H20FNO3 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 C19H20FNO3 suppliers with JDMF on PharmaCompass.
We have 8 companies offering C19H20FNO3
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