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01 1Active Pharma Inc.

02 1Assia Chemical Industries Ltd.

03 1Daito Co., Ltd.

04 1JUBILANT PHARMOVA LIMITED

05 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.

06 1Shijiazhuang Lonzeal Pharmaceuticals Co. , Ltd.

07 1Sumitomo Chemical Co., Ltd.

08 1Zydus Lifesciences Limited

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PharmaCompass

01

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Paroxetine hydrochloride hydrate "Teva"

Registration Number : 223MF10002

Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel

Initial Date of Registration : 2011-01-07

Latest Date of Registration : 2011-11-17

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02

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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

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03

PharmaVenue
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Paroxetine Hydrochloride Hydrate

Registration Number : 231MF10081

Registrant's Address : 1A, Sector 16A, Noida 201 301, Uttar Pradesh, India

Initial Date of Registration : 2019-04-03

Latest Date of Registration : 2019-04-03

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04

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Japanese Pharmacopoeia Paroxetine Hydrochloride Hydrate For manufacturing 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

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05

PharmaVenue
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Paroxetine hydrochloride hydrate

Registration Number : 222MF10283

Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo

Initial Date of Registration : 2010-12-27

Latest Date of Registration : 2012-10-01

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06

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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

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07

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08

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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

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Paroxetine Hydrochloride Hemihydrate Manufacturers

A Paroxetine Hydrochloride Hemihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paroxetine Hydrochloride Hemihydrate, including repackagers and relabelers. The FDA regulates Paroxetine Hydrochloride Hemihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paroxetine Hydrochloride Hemihydrate 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 Paroxetine Hydrochloride Hemihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Paroxetine Hydrochloride Hemihydrate Suppliers

A Paroxetine Hydrochloride Hemihydrate supplier is an individual or a company that provides Paroxetine Hydrochloride Hemihydrate active pharmaceutical ingredient (API) or Paroxetine Hydrochloride Hemihydrate finished formulations upon request. The Paroxetine Hydrochloride Hemihydrate suppliers may include Paroxetine Hydrochloride Hemihydrate API manufacturers, exporters, distributors and traders.

click here to find a list of Paroxetine Hydrochloride Hemihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Paroxetine Hydrochloride Hemihydrate JDMF

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 Paroxetine Hydrochloride Hemihydrate Drug Master File in Japan (Paroxetine Hydrochloride Hemihydrate JDMF) empowers Paroxetine Hydrochloride Hemihydrate 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 Paroxetine Hydrochloride Hemihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Paroxetine Hydrochloride Hemihydrate 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 Paroxetine Hydrochloride Hemihydrate suppliers with JDMF on PharmaCompass.

Paroxetine Hydrochloride Hemihydrate Manufacturers | Traders | Suppliers

Paroxetine Hydrochloride Hemihydrate Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.