Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 2Chunghwa Chemical Synthesis & Biotech Co., Ltd. Shu-Lin TW
02 1BIOCON LIMITED Bengaluru IN
03 2CONCORD BIOTECH LIMITED Ahmedabad IN
04 1Hisun Pharmaceutical (Hangzhou) Co., Ltd. Hangzhou City CN
05 1JOYANG LABORATORIES Yancheng CN
06 1LEK PHARMACEUTICALS D.D. Ljubljana SI
07 1North China Pharmaceutical Huasheng Co., Ltd. Shijiazhuang CN
08 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
09 1WUXI FORTUNE PHARMACEUTICAL CO., LTD. Wuxi CN
01 9Tacrolimus monohydrate
02 1Tacrolimus monohydrate, Process B
03 1Tacrolimus monohydrate, Process II
01 4China
02 3India
03 1Israel
04 1Slovenia
05 2Taiwan
01 11Valid
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Certificate Number : CEP 2018-241 - Rev 02
Status : Valid
Issue Date : 2024-12-20
Type : Chemical
Substance Number : 2244
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Tacrolimus Monohydrate, Process B
Certificate Number : CEP 2023-345 - Rev 00
Status : Valid
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 2244
Certificate Number : CEP 2017-257 - Rev 01
Status : Valid
Issue Date : 2023-11-29
Type : Chemical
Substance Number : 2244
Certificate Number : R0-CEP 2018-216 - Rev 00
Status : Valid
Issue Date : 2020-06-02
Type : Chemical
Substance Number : 2244
Tacrolimus Monohydrate, Process II
Certificate Number : R0-CEP 2020-227 - Rev 01
Status : Valid
Issue Date : 2022-12-19
Type : Chemical
Substance Number : 2244
Certificate Number : CEP 2021-210 - Rev 01
Status : Valid
Issue Date : 2024-07-22
Type : Chemical and TSE
Substance Number : 2244
Certificate Number : R0-CEP 2021-204 - Rev 01
Status : Valid
Issue Date : 2023-08-07
Type : Chemical
Substance Number : 2244
Certificate Number : R0-CEP 2021-180 - Rev 01
Status : Valid
Issue Date : 2023-06-19
Type : Chemical
Substance Number : 2244
Certificate Number : CEP 2018-233 - Rev 04
Status : Valid
Issue Date : 2024-08-05
Type : Chemical
Substance Number : 2244
Certificate Number : CEP 2018-284 - Rev 02
Status : Valid
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 2244
A Tacrolimus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tacrolimus, including repackagers and relabelers. The FDA regulates Tacrolimus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tacrolimus 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 Tacrolimus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tacrolimus supplier is an individual or a company that provides Tacrolimus active pharmaceutical ingredient (API) or Tacrolimus finished formulations upon request. The Tacrolimus suppliers may include Tacrolimus API manufacturers, exporters, distributors and traders.
click here to find a list of Tacrolimus suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tacrolimus CEP of the European Pharmacopoeia monograph is often referred to as a Tacrolimus Certificate of Suitability (COS). The purpose of a Tacrolimus CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tacrolimus EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tacrolimus to their clients by showing that a Tacrolimus CEP has been issued for it. The manufacturer submits a Tacrolimus CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tacrolimus CEP holder for the record. Additionally, the data presented in the Tacrolimus CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tacrolimus DMF.
A Tacrolimus CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tacrolimus CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Tacrolimus suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Tacrolimus
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