Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim S. A.
02 1Pharmaceutical Works POLPHARMA S. A.
03 1Glenmark Life Sciences Limited
04 1Honor Lab Limited
05 1Ryoto Fine Co., Ltd.
06 1SMS Pharmaceuticals Limited
07 1Tianish Laboratories Private Limited
08 1Topharman Shandong Co. ,Ltd
01 6Tadalafil
02 1Tadalafil
03 1Tadalafil [D]
01 1China
02 3India
03 1Japan
04 1Poland
05 1Spain
06 1U.S.A
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Registration Number : 230MF10089
Registrant's Address : Joan Buscala, 10 E-08173 Sant Cugat del Valles, Barcelona, Spain
Initial Date of Registration : 2018-07-20
Latest Date of Registration : 2018-07-20
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 302MF10011
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2020-01-24
Latest Date of Registration : 2024-06-06
Registration Number : 231MF10055
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2019-02-25
Latest Date of Registration : 2019-02-25
Registration Number : 230MF10172
Registrant's Address : H. No. &8-3-166/7/1, Erragadda, Hyderabad-500018, Telangana, INDIA.
Initial Date of Registration : 2018-12-21
Latest Date of Registration : 2018-12-21
Registration Number : 227MF10192
Registrant's Address : 1410 Takada, Kashiwa City, Chiba Prefecture
Initial Date of Registration : 2015-08-03
Latest Date of Registration : 2016-11-22
Registration Number : 231MF10041
Registrant's Address : Plot No. 72, H. No.8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills,...
Initial Date of Registration : 2019-02-13
Latest Date of Registration : 2023-11-15
Tadalafil "For manufacturing purposes only"
Registration Number : 231MF10002
Registrant's Address : 49 Wenshuibeilu, Xin'an District, Anqiu City, Weifang City, Shandong Province, China
Initial Date of Registration : 2019-01-10
Latest Date of Registration : 2019-01-10
Registration Number : 230MF10148
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2018-11-05
Latest Date of Registration : 2023-10-12
A Cialis manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cialis, including repackagers and relabelers. The FDA regulates Cialis manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cialis 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 Cialis manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cialis supplier is an individual or a company that provides Cialis active pharmaceutical ingredient (API) or Cialis finished formulations upon request. The Cialis suppliers may include Cialis API manufacturers, exporters, distributors and traders.
click here to find a list of Cialis 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 Cialis Drug Master File in Japan (Cialis JDMF) empowers Cialis 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 Cialis JDMF during the approval evaluation for pharmaceutical products. At the time of Cialis 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 Cialis suppliers with JDMF on PharmaCompass.
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