TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TEVA PHARMACEUTICAL INDUSTRIES LTD Petach Tikva IL
02 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
03 1ANUH PHARMA LTD. Mumbai IN
04 2HEC PHARM CO., LTD. Yidu City CN
05 1JUBILANT PHARMOVA LIMITED Nanjangud IN
06 1Nexchem Pharmaceutical Co., Ltd. Jinhua City CN
07 1PLIVA CROATIA LTD. Zagreb HR
08 1SANDOZ INDUSTRIAL PRODUCTS S.A. Les Franqueses Del Vallès ES
01 2Azithromycin
02 6Azithromycin, Monohydrate
03 1Azithromycin, PII
01 3China
02 1Croatia
03 1Germany
04 3India
05 1Israel
01 6Valid
02 3Withdrawn by Holder
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2004-181 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2020-02-03
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2014-118 - Rev 01
Status : Valid
Issue Date : 2023-03-10
Type : Chemical
Substance Number : 1649
Certificate Number : CEP 2021-143 - Rev 01
Status : Valid
Issue Date : 2025-01-22
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2014-185 - Rev 00
Status : Valid
Issue Date : 2020-08-28
Type : Chemical
Substance Number : 1649
Certificate Number : R0-CEP 2017-154 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2017-10-26
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2007-118 - Rev 05
Status : Valid
Issue Date : 2022-08-12
Type : Chemical
Substance Number : 1649
Certificate Number : CEP 2021-069 - Rev 00
Status : Valid
Issue Date : 2023-09-20
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2010-131 - Rev 02
Status : Valid
Issue Date : 2021-10-27
Type : Chemical
Substance Number : 1649
Certificate Number : R1-CEP 2002-257 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2012-09-26
Type : Chemical
Substance Number : 1649
64
PharmaCompass offers a list of Azithromycin 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 manufacturer or Azithromycin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azithromycin manufacturer or Azithromycin supplier.
PharmaCompass also assists you with knowing the Azithromycin API Price utilized in the formulation of products. Azithromycin API Price is not always fixed or binding as the Azithromycin Price is obtained through a variety of data sources. The Azithromycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ultreon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ultreon, including repackagers and relabelers. The FDA regulates Ultreon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ultreon 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 Ultreon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ultreon supplier is an individual or a company that provides Ultreon active pharmaceutical ingredient (API) or Ultreon finished formulations upon request. The Ultreon suppliers may include Ultreon API manufacturers, exporters, distributors and traders.
click here to find a list of Ultreon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ultreon CEP of the European Pharmacopoeia monograph is often referred to as a Ultreon Certificate of Suitability (COS). The purpose of a Ultreon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ultreon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ultreon to their clients by showing that a Ultreon CEP has been issued for it. The manufacturer submits a Ultreon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ultreon CEP holder for the record. Additionally, the data presented in the Ultreon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ultreon DMF.
A Ultreon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ultreon 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 Ultreon suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Ultreon
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