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01 1Interquim S. A.

02 1AGC Pharma Chemicals Europe, S. L. U.

03 1Active Pharma Inc.

04 1Alembic Pharmaceuticals Limited

05 1Assia Chemical Industries Ltd.

06 1DONGBANG FUTURE TECH & LIFE CO. , LTD.

07 1Daiwa Pharmaceutical Industries Co., Ltd.

08 2Glenmark Life Sciences Limited

09 1Inke S.A.

10 1JUBILANT PHARMOVA LIMITED

11 1Jiangsu Zhongbang Pharmaceutical Co. , Ltd.

12 1Kyongbo Pharmaceutical Co. , Ltd.

13 1LUPIN LIMITED.

14 1Shin Poong Pharm. Co. , Ltd.

15 1Sumitomo Chemical Co., Ltd.

16 1Topharman Shandong Co. ,Ltd

17 1Yoshindo Co., Ltd.

18 1Zhejiang Apeloa Jiayuan Pharmaceutical Co. , Ltd.

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PharmaCompass

01

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothInterquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

Telmisartan

Registration Number : 226MF10144

Registrant's Address : Joan Buscala, 10 E-08173 Sant Cugat del Valles, Barcelona, ​​Spain

Initial Date of Registration : 2014-07-31

Latest Date of Registration : 2015-11-19

Interquim

02

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Telmisartan

Registration Number : 228MF10015

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

Initial Date of Registration : 2016-01-08

Latest Date of Registration : 2023-06-07

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03

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Telmisartan

Registration Number : 302MF10080

Registrant's Address : Cami(´) de la Pomereda, 13, Malgrat de Mar, Barcelona, ​​08380, Espan(~)a

Initial Date of Registration : 2020-07-09

Latest Date of Registration : 2020-07-09

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05

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Telmisartan

Registration Number : 230MF10082

Registrant's Address : 36 Shuanggao Rd. , Gaochun, Nanjing, Jiangsu, China

Initial Date of Registration : 2018-07-09

Latest Date of Registration : 2018-07-09

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06

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Telmisartan

Registration Number : 228MF10059

Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...

Initial Date of Registration : 2016-02-24

Latest Date of Registration : 2016-11-22

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09

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Telmisartan "For manufacturing purposes only"

Registration Number : 228MF10071

Registrant's Address : 49 Wenshuibeilu, Xin'an District, Anqiu City, Weifang City, Shandong Province, China

Initial Date of Registration : 2016-03-02

Latest Date of Registration : 2021-03-17

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Inke S.A.

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Inke S.A.

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Telmisartan

Registration Number : 228MF10056

Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN

Initial Date of Registration : 2016-02-18

Latest Date of Registration : 2016-11-22

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Telmisartan Manufacturers

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

Telmisartan Suppliers

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

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

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

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.