01 1ARAGEN LIFE SCIENCES LIMITED.
02 1JUBILANT PHARMOVA LIMITED
03 1Proto Chemicals AG
04 1SUN PHARMACEUTICAL INDUSTRIES LTD.
05 1Saneca Pharmaceuticals a. s.
06 1Tateyama Chemical Co., Ltd.
07 1Zydus Cadila Healthcare Ltd.
01 2Tramadol Hydrochloride
02 4Tramadol hydrochloride
03 1Tramadol hydrochloride "Tateyama"
01 1Germany
02 4India
03 1Japan
04 1Slovakia
Registration Number : 229MF10118
Registrant's Address : 28A, IDA, Nacharam Hyderabad Telangana, India
Initial Date of Registration : 2017-07-10
Latest Date of Registration : 2017-07-10
Registration Number : 218MF10134
Registrant's Address : Tschachen 2, 8756 Mitloedi (Glarus Sued), Switzerland
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2008-02-25
Registration Number : 229MF10160
Registrant's Address : 1A, Sector 16A, Noida 201 301, Uttar Pradesh, India
Initial Date of Registration : 2017-08-17
Latest Date of Registration : 2018-05-08
Registration Number : 229MF10138
Registrant's Address : Nitrianska 100,920 27 Hlohovec, Slovak Republic
Initial Date of Registration : 2017-07-24
Latest Date of Registration : 2022-03-24
Registration Number : 226MF10018
Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...
Initial Date of Registration : 2014-01-21
Latest Date of Registration : 2015-03-06
Tramadol hydrochloride "Tateyama"
Registration Number : 228MF10189
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2016-09-30
Latest Date of Registration : 2018-05-21
Registration Number : 301MF10065
Registrant's Address : “Zydus Tower”, Satellite Cross Roads, Ahmedabad 380015, India
Initial Date of Registration : 2019-09-17
Latest Date of Registration : 2019-11-15
A Tramadol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tramadol, including repackagers and relabelers. The FDA regulates Tramadol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tramadol 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 Tramadol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tramadol supplier is an individual or a company that provides Tramadol active pharmaceutical ingredient (API) or Tramadol finished formulations upon request. The Tramadol suppliers may include Tramadol API manufacturers, exporters, distributors and traders.
click here to find a list of Tramadol 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 Tramadol Drug Master File in Japan (Tramadol JDMF) empowers Tramadol 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 Tramadol JDMF during the approval evaluation for pharmaceutical products. At the time of Tramadol 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 Tramadol suppliers with JDMF on PharmaCompass.
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