01 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
02 1CSPC OUYI PHARMACEUTICAL CO., LTD. Shijiazhuang CN
03 1ERCROS S.A. Aranjuez ES
04 1HEC PHARM CO., LTD. Yidu City CN
05 1HUANGSHI SHIXING PHARMACEUTICAL CO., LTD. Huangshi CN
06 1JIANGSU WEIQIDA PHARMACEUTICAL CO., LTD. Nantong City CN
07 1JUBILANT PHARMOVA LIMITED Nanjangud IN
08 1KOPRAN RESEARCH LABORATORIES LIMITED Mumbai IN
09 1NINGXIA TAIYICIN BIOTECH CO., LTD. Yinchuan City CN
10 1Ningxia Qiyuan Pharmaceutical Co., Ltd. Yinchuan City CN
11 1TAPI NL B.V. Amsterdam NL
12 1ZHEJIANG GUOBANG PHARMACEUTICAL CO., LTD. Shangyu CN
01 12Azithromycin, Dihydrate
01 7China
02 3India
03 1Spain
04 1Blank
01 12Valid
Certificate Number : R1-CEP 2007-165 - Rev 04
Status : Valid
Issue Date : 2022-04-06
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2008-315 - Rev 04
Status : Valid
Issue Date : 2019-09-12
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2007-206 - Rev 03
Status : Valid
Issue Date : 2022-02-04
Type : Chemical
Substance Number : 1649
Certificate Number : R0-CEP 2021-114 - Rev 00
Status : Valid
Issue Date : 2023-07-31
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2007-119 - Rev 06
Status : Valid
Issue Date : 2022-09-29
Type : Chemical
Substance Number : 1649
Certificate Number : CEP 2005-230 - Rev 03
Status : Valid
Issue Date : 2024-04-02
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2012-212 - Rev 00
Status : Valid
Issue Date : 2018-12-14
Type : Chemical
Substance Number : 1649
Certificate Number : CEP 2021-443 - Rev 00
Status : Valid
Issue Date : 2024-02-23
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2013-153 - Rev 03
Status : Valid
Issue Date : 2023-08-10
Type : Chemical
Substance Number : 1649
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2007-072 - Rev 03
Status : Valid
Issue Date : 2025-01-03
Type : Chemical
Substance Number : 1649
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
29
PharmaCompass offers a list of Azithromycin Dihydrate 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 Azithromycin Dihydrate manufacturer or Azithromycin Dihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azithromycin Dihydrate manufacturer or Azithromycin Dihydrate supplier.
PharmaCompass also assists you with knowing the Azithromycin Dihydrate API Price utilized in the formulation of products. Azithromycin Dihydrate API Price is not always fixed or binding as the Azithromycin Dihydrate Price is obtained through a variety of data sources. The Azithromycin Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Azitrox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azitrox, including repackagers and relabelers. The FDA regulates Azitrox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azitrox 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 Azitrox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azitrox supplier is an individual or a company that provides Azitrox active pharmaceutical ingredient (API) or Azitrox finished formulations upon request. The Azitrox suppliers may include Azitrox API manufacturers, exporters, distributors and traders.
click here to find a list of Azitrox suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Azitrox CEP of the European Pharmacopoeia monograph is often referred to as a Azitrox Certificate of Suitability (COS). The purpose of a Azitrox CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Azitrox EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Azitrox to their clients by showing that a Azitrox CEP has been issued for it. The manufacturer submits a Azitrox CEP (COS) as part of the market authorization procedure, and it takes on the role of a Azitrox CEP holder for the record. Additionally, the data presented in the Azitrox CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Azitrox DMF.
A Azitrox CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Azitrox 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 Azitrox suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Azitrox
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