01 1Active Pharma Co., Ltd.
02 1Aurobindo Pharma Limited
03 1HETERO DRUGS LIMITED.
04 1Matrix Pharmacorp Private Limited
05 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
06 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
07 1SperaNexus Co., Ltd.
01 1Sertraline Hydrochloride
02 5Sertraline hydrochloride
03 1Sertraline hydrochloride salt production dedicated
01 2India
02 1Italy
03 3Japan
04 1U.S.A
Registration Number : 226MF10098
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Telangana, India
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2015-04-22
Registration Number : 226MF10175
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2020-07-16
Registration Number : 226MF10149
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2015-05-14
Sertraline hydrochloride For manufacturing purposes only
Registration Number : 226MF10157
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2014-09-01
Registration Number : 226MF10095
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2014-05-14
Registration Number : 226MF10137
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2014-07-31
Latest Date of Registration : 2015-05-12
Registration Number : 225MF10221
Registrant's Address : Plot No. 14, 99 and 100, IDA, Pashamylaram Phase-II, Patancheru, Sangareddy District ...
Initial Date of Registration : 2013-12-03
Latest Date of Registration : 2013-12-03
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PharmaCompass offers a list of Sertraline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Sertraline Hydrochloride manufacturer or Sertraline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sertraline Hydrochloride manufacturer or Sertraline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Sertraline Hydrochloride API Price utilized in the formulation of products. Sertraline Hydrochloride API Price is not always fixed or binding as the Sertraline Hydrochloride Price is obtained through a variety of data sources. The Sertraline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sealdin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sealdin, including repackagers and relabelers. The FDA regulates Sealdin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sealdin 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 Sealdin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sealdin supplier is an individual or a company that provides Sealdin active pharmaceutical ingredient (API) or Sealdin finished formulations upon request. The Sealdin suppliers may include Sealdin API manufacturers, exporters, distributors and traders.
click here to find a list of Sealdin 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 Sealdin Drug Master File in Japan (Sealdin JDMF) empowers Sealdin 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 Sealdin JDMF during the approval evaluation for pharmaceutical products. At the time of Sealdin 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 Sealdin suppliers with JDMF on PharmaCompass.
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