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
24
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 Azitral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azitral, including repackagers and relabelers. The FDA regulates Azitral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azitral 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 Azitral manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azitral supplier is an individual or a company that provides Azitral active pharmaceutical ingredient (API) or Azitral finished formulations upon request. The Azitral suppliers may include Azitral API manufacturers, exporters, distributors and traders.
click here to find a list of Azitral suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Azitral CEP of the European Pharmacopoeia monograph is often referred to as a Azitral Certificate of Suitability (COS). The purpose of a Azitral CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Azitral EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Azitral to their clients by showing that a Azitral CEP has been issued for it. The manufacturer submits a Azitral CEP (COS) as part of the market authorization procedure, and it takes on the role of a Azitral CEP holder for the record. Additionally, the data presented in the Azitral CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Azitral DMF.
A Azitral CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Azitral 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 Azitral suppliers with CEP (COS) on PharmaCompass.
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