01 1Fujian Fukang Pharmaceutical Co., Ltd. Fuzhou City CN
02 1JINHE BIOTECHNOLOGY CO., LTD. Huhhot CN
03 1PUCHENG CHIA TAI BIOCHEMISTRY CO., LTD. Pucheng County CN
01 1Chlortetracycline hydrochloride
02 1Chlortetracycline hydrochloride, For veterinary use only
03 1Chlortetracycline hydrochloride, For veterinary use only, CTC.HCl (non-micronised), Super CTC.HCl (micronised)
01 3China
01 3Valid
Chlortetracycline Hydrochloride
Certificate Number : R1-CEP 2005-110 - Rev 03
Status : Valid
Issue Date : 2018-10-22
Type : Chemical
Substance Number : 173
Chlortetracycline Hydrochloride, For Veterinary ...
Certificate Number : R1-CEP 2007-291 - Rev 00
Status : Valid
Issue Date : 2014-07-10
Type : Chemical
Substance Number : 173
Chlortetracycline Hydrochloride, For Veterinary ...
Certificate Number : R1-CEP 2002-195 - Rev 04
Status : Valid
Issue Date : 2021-09-23
Type : Chemical
Substance Number : 173
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PharmaCompass offers a list of Chlortetracycline Hydrochloride 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 Chlortetracycline Hydrochloride manufacturer or Chlortetracycline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlortetracycline Hydrochloride manufacturer or Chlortetracycline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Chlortetracycline Hydrochloride API Price utilized in the formulation of products. Chlortetracycline Hydrochloride API Price is not always fixed or binding as the Chlortetracycline Hydrochloride Price is obtained through a variety of data sources. The Chlortetracycline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aureomycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aureomycin, including repackagers and relabelers. The FDA regulates Aureomycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aureomycin 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 Aureomycin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aureomycin supplier is an individual or a company that provides Aureomycin active pharmaceutical ingredient (API) or Aureomycin finished formulations upon request. The Aureomycin suppliers may include Aureomycin API manufacturers, exporters, distributors and traders.
click here to find a list of Aureomycin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aureomycin CEP of the European Pharmacopoeia monograph is often referred to as a Aureomycin Certificate of Suitability (COS). The purpose of a Aureomycin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aureomycin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aureomycin to their clients by showing that a Aureomycin CEP has been issued for it. The manufacturer submits a Aureomycin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aureomycin CEP holder for the record. Additionally, the data presented in the Aureomycin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aureomycin DMF.
A Aureomycin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aureomycin CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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