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 1TAPI NL B.V. Amsterdam NL
09 1WUXI FORTUNE PHARMACEUTICAL CO., LTD. Wuxi CN
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.
Tacrolimus Monohydrate, Process B
Certificate Number : CEP 2023-345 - Rev 00
Status : Valid
Issue Date : 2024-03-28
Type : Chemical
Substance Number : 2244
100
PharmaCompass offers a list of Tacrolimus 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 Tacrolimus manufacturer or Tacrolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tacrolimus manufacturer or Tacrolimus supplier.
PharmaCompass also assists you with knowing the Tacrolimus API Price utilized in the formulation of products. Tacrolimus API Price is not always fixed or binding as the Tacrolimus Price is obtained through a variety of data sources. The Tacrolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Astagraf XL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Astagraf XL, including repackagers and relabelers. The FDA regulates Astagraf XL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Astagraf XL API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Astagraf XL supplier is an individual or a company that provides Astagraf XL active pharmaceutical ingredient (API) or Astagraf XL finished formulations upon request. The Astagraf XL suppliers may include Astagraf XL API manufacturers, exporters, distributors and traders.
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A Astagraf XL CEP of the European Pharmacopoeia monograph is often referred to as a Astagraf XL Certificate of Suitability (COS). The purpose of a Astagraf XL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Astagraf XL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Astagraf XL to their clients by showing that a Astagraf XL CEP has been issued for it. The manufacturer submits a Astagraf XL CEP (COS) as part of the market authorization procedure, and it takes on the role of a Astagraf XL CEP holder for the record. Additionally, the data presented in the Astagraf XL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Astagraf XL DMF.
A Astagraf XL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Astagraf XL 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 Astagraf XL suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Astagraf XL
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