DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 1FERMION OY Espoo FI
03 1COHANCE LIFESCIENCES LIMITED Mumbai IN
04 1EGIS Pharmaceuticals PLC Budapest HU
05 1IOL CHEMICALS AND PHARMACEUTICALS LTD Ludhiana IN
06 2Moehs Iberica S.L. Rubi ES
07 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
08 2TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
09 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
10 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
11 1DIVI'S LABORATORIES LIMITED Hyderabad IN
12 1HETERO LABS LIMITED Hyderabad IN
13 1HIKAL LIMITED Bangalore IN
14 1INDOCO REMEDIES LIMITED Mumbai IN
15 2IPCA LABORATORIES LIMITED Mumbai IN
16 1JUBILANT PHARMOVA LIMITED Nanjangud IN
17 1LUPIN LIMITED Mumbai IN
18 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
19 1MEGAFINE PHARMA (P) LIMITED Mumbai IN
20 1MENADIONA, S.L. Palafolls ES
21 1Medichem, S.A. Sant Joan Despí ES
22 2NIFTY LABS PVT. LTD. Hyderabad IN
23 2NOSCH LABS PRIVATE LIMITED Hyderabad IN
24 2OLON S.P.A. Rodano IT
25 1RAKS PHARMA PVT. LTD. Visakhapatnam IN
26 1SHANDONG ANXIN PHARMACEUTICAL CO., LTD. Dongjia Town CN
27 1SYNTHIMED LABS PRIVATE LIMITED Derabassi IN
28 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
29 1Unichem Laboratories Limited Mumbai IN
30 2Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
31 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
32 1ZHEJIANG HISOAR PHARMACEUTICAL CO., LTD. Taizhou CN
33 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
34 1Zhejiang Supor Pharmaceuticals Co., Ltd. Shaoxing CN
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : CEP 2014-200 - Rev 01
Status : Valid
Issue Date : 2024-03-15
Type : Chemical
Substance Number : 2541
With Fermion, start the journey of your innovative API.
Certificate Number : CEP 2015-170 - Rev 01
Status : Valid
Issue Date : 2023-10-16
Type : Chemical
Substance Number : 2541
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2017-175 - Rev 01
Status : Valid
Issue Date : 2024-07-09
Type : Chemical
Substance Number : 2541
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 2016-049 - Rev 00
Status : Valid
Issue Date : 2022-07-27
Type : Chemical
Substance Number : 2541
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Certificate Number : CEP 2023-102 - Rev 00
Status : Valid
Issue Date : 2025-03-04
Type : Chemical
Substance Number : 2541
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 2014-287 - Rev 00
Status : Valid
Issue Date : 2021-03-08
Type : Chemical
Substance Number : 2541
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R0-CEP 2019-291 - Rev 02
Status : Valid
Issue Date : 2023-07-10
Type : Chemical
Substance Number : 2541
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2020-234 - Rev 02
Status : Valid
Issue Date : 2023-12-19
Type : Chemical
Substance Number : 2541
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2017-210 - Rev 04
Status : Valid
Issue Date : 2024-04-17
Type : Chemical
Substance Number : 2541
88
PharmaCompass offers a list of Quetiapine Fumarate 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 Quetiapine Fumarate manufacturer or Quetiapine Fumarate supplier for your needs.
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A Quetiapine Fumarate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quetiapine Fumarate, including repackagers and relabelers. The FDA regulates Quetiapine Fumarate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quetiapine Fumarate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Quetiapine Fumarate supplier is an individual or a company that provides Quetiapine Fumarate active pharmaceutical ingredient (API) or Quetiapine Fumarate finished formulations upon request. The Quetiapine Fumarate suppliers may include Quetiapine Fumarate API manufacturers, exporters, distributors and traders.
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A Quetiapine Fumarate CEP of the European Pharmacopoeia monograph is often referred to as a Quetiapine Fumarate Certificate of Suitability (COS). The purpose of a Quetiapine Fumarate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Quetiapine Fumarate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Quetiapine Fumarate to their clients by showing that a Quetiapine Fumarate CEP has been issued for it. The manufacturer submits a Quetiapine Fumarate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Quetiapine Fumarate CEP holder for the record. Additionally, the data presented in the Quetiapine Fumarate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Quetiapine Fumarate DMF.
A Quetiapine Fumarate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Quetiapine Fumarate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 34 companies offering Quetiapine Fumarate
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