IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
02 2EGIS Pharmaceuticals PLC Budapest HU
03 3TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
04 1ANUH PHARMA LTD. Mumbai IN
05 1CHONGQING QINGYANG PHARMACEUTICAL CO., LTD. Chongqing CN
06 1EXEMED PHARMACEUTICALS Vadodara IN
07 1HARMAN FINOCHEM LIMITED Mumbai IN
08 1HETERO DRUGS LIMITED Hyderabad IN
09 1INDOCO REMEDIES LIMITED Mumbai IN
10 1IPCA Laboratories Limited Mumbai IN
11 1Kraemer & Martin Pharma Handels GmbH Krefeld DE
12 1MANGALAM DRUGS & ORGANICS LTD. Mumbai IN
13 1SIGNA S.A. DE C.V. Toluca MX
14 1SINBIOTIK S.A. DE C.V. Tlalnepantla de Baz MX
15 1SMS LIFESCIENCES INDIA LIMITED Hyderabad IN
16 1STYRAX PHARMA PRIVATE LIMITED Anakapalli IN
17 1Shanghai OSD Co., Ltd. Shanghai CN
18 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
19 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
01 20Allopurinol
02 1Allopurinol, Allopurinol P-process
03 1Allopurinol, Synthetic route B
01 2China
02 1Germany
03 2Hungary
04 11India
05 3Israel
06 2Mexico
07 1Spain
01 1Expired
02 18Valid
03 1Withdrawn by EDQM Failure to CEP procedure
04 2Withdrawn by Holder
Certificate Number : CEP 2023-029 - Rev 00
Status : Valid
Issue Date : 2024-06-10
Type : Chemical
Substance Number : 576
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Allopurinol, Synthetic Route B
Certificate Number : CEP 2014-364 - Rev 01
Status : Valid
Issue Date : 2023-11-27
Type : Chemical
Substance Number : 576
Certificate Number : R1-CEP 1999-007 - Rev 07
Status : Valid
Issue Date : 2023-07-21
Type : Chemical
Substance Number : 576
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : R1-CEP 1996-032 - Rev 05
Status : Valid
Issue Date : 2019-08-09
Type : Chemical
Substance Number : 576
Allopurinol, Allopurinol P-process
Certificate Number : CEP 2014-117 - Rev 02
Status : Valid
Issue Date : 2024-02-16
Type : Chemical
Substance Number : 576
Certificate Number : CEP 2001-433 - Rev 05
Status : Valid
Issue Date : 2024-03-11
Type : Chemical
Substance Number : 576
Certificate Number : CEP 2008-017 - Rev 04
Status : Valid
Issue Date : 2023-11-20
Type : Chemical
Substance Number : 576
Certificate Number : CEP 2021-239 - Rev 01
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 576
Certificate Number : R0-CEP 2022-119 - Rev 00
Status : Valid
Issue Date : 2023-06-20
Type : Chemical
Substance Number : 576
Certificate Number : CEP 2000-015 - Rev 07
Status : Valid
Issue Date : 2024-07-25
Type : Chemical
Substance Number : 576
A Allopurinol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allopurinol, including repackagers and relabelers. The FDA regulates Allopurinol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allopurinol 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 Allopurinol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Allopurinol supplier is an individual or a company that provides Allopurinol active pharmaceutical ingredient (API) or Allopurinol finished formulations upon request. The Allopurinol suppliers may include Allopurinol API manufacturers, exporters, distributors and traders.
click here to find a list of Allopurinol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Allopurinol CEP of the European Pharmacopoeia monograph is often referred to as a Allopurinol Certificate of Suitability (COS). The purpose of a Allopurinol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Allopurinol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Allopurinol to their clients by showing that a Allopurinol CEP has been issued for it. The manufacturer submits a Allopurinol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Allopurinol CEP holder for the record. Additionally, the data presented in the Allopurinol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Allopurinol DMF.
A Allopurinol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Allopurinol 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 Allopurinol suppliers with CEP (COS) on PharmaCompass.
We have 19 companies offering Allopurinol
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