TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
02 1ABC Farmaceutici S.p.A. Torino IT
03 1ABC Farmaceutici S.p.A. Trecate IT
04 2AURORE LIFE SCIENCES PRIVATE LIMITED Hyderabad IN
05 1EXCELLA GMBH & CO. KG Feucht DE
06 1HETERO DRUGS LIMITED Hyderabad IN
07 1HUBEI YITAI PHARMACEUTICAL CO., LTD. Tianmen city CN
08 1MANGALAM DRUGS & ORGANICS LTD. Mumbai IN
09 2OLON S.P.A. Rodano IT
10 1QUIMICA SINTETICA S.A. Alcala De Henares ES
11 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S.P.A. Milano IT
12 1Ranbaxy Laboratories Limited Dewas IN
13 1Recordati S.p.A. Milano IT
14 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
15 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
16 1Vorin Laboratories Ltd Secunderabad IN
17 1ZHEJIANG CHARIOTEER PHARMACEUTICAL CO., LTD Xianju CN
18 1ZHEJIANG ZHEBEI PHARMACEUTICAL CO., LTD Xinshi Town, Deqing CN
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Certificate Number : CEP 1997-084 - Rev 12
Status : Valid
Issue Date : 2024-05-30
Type : Chemical
Substance Number : 968
A Aciclovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aciclovir, including repackagers and relabelers. The FDA regulates Aciclovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aciclovir 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 Aciclovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aciclovir supplier is an individual or a company that provides Aciclovir active pharmaceutical ingredient (API) or Aciclovir finished formulations upon request. The Aciclovir suppliers may include Aciclovir API manufacturers, exporters, distributors and traders.
click here to find a list of Aciclovir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aciclovir CEP of the European Pharmacopoeia monograph is often referred to as a Aciclovir Certificate of Suitability (COS). The purpose of a Aciclovir CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aciclovir EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aciclovir to their clients by showing that a Aciclovir CEP has been issued for it. The manufacturer submits a Aciclovir CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aciclovir CEP holder for the record. Additionally, the data presented in the Aciclovir CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aciclovir DMF.
A Aciclovir CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aciclovir 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 Aciclovir suppliers with CEP (COS) on PharmaCompass.
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