EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI GERMANY GmbH Frankfurt am Main DE
02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
03 2USV PRIVATE LIMITED Mumbai IN
04 1Chongqing Carelife Pharmaceutical Co. Ltd. Chongqing CN
05 1DISHMAN CARBOGEN AMCIS LIMITED Ahmedabad IN
06 1EDMOND PHARMA S.R.L. Paderno Dugnano IT
07 2GLENMARK LIFE SCIENCES LIMITED Mumbai IN
08 1HETERO DRUGS LIMITED Hyderabad IN
09 1INDOCO REMEDIES LIMITED Mumbai IN
10 1INIST ST CO., LTD. Eumseong-gun KR
11 1IPCA Laboratories Limited Mumbai IN
12 1KORES (INDIA) LIMITED Navi Mumbai IN
13 1MEDILUX LABORATORIES PRIVATE LIMITED Pithampur IN
14 1MICRO LABS LIMITED Bengaluru IN
15 1MSN LIFE SCIENCES PRIVATE LIMITED Bhiknoor Village IN
16 1Nexchem Pharmaceutical Co., Ltd. Jinhua City CN
17 1Oman Chemicals And Pharmaceuticals L.L.C. Al Buraimi OM
18 1SHENZHEN HAORUI INDUSTRIAL DEV. CO., LTD. Shenzhen CN
19 1URQUIMA S.A. Palau-solità i Plegamans ES
20 1ZENTIVA K.S. Praha 10 CZ
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2005-150 - Rev 03
Status : Valid
Issue Date : 2021-12-09
Type : Chemical
Substance Number : 2223
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2008-072 - Rev 05
Status : Valid
Issue Date : 2022-03-08
Type : Chemical
Substance Number : 2223
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Certificate Number : R1-CEP 2006-243 - Rev 05
Status : Valid
Issue Date : 2022-05-17
Type : Chemical
Substance Number : 2223
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R0-CEP 2022-234 - Rev 00
Status : Valid
Issue Date : 2022-10-10
Type : Chemical
Substance Number : 2223
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Certificate Number : CEP 2023-130 - Rev 00
Status : Valid
Issue Date : 2023-11-07
Type : Chemical
Substance Number : 2223
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PharmaCompass offers a list of Glimepiride 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 Glimepiride manufacturer or Glimepiride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glimepiride manufacturer or Glimepiride supplier.
PharmaCompass also assists you with knowing the Glimepiride API Price utilized in the formulation of products. Glimepiride API Price is not always fixed or binding as the Glimepiride Price is obtained through a variety of data sources. The Glimepiride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glimepiride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glimepiride, including repackagers and relabelers. The FDA regulates Glimepiride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glimepiride 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 Glimepiride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glimepiride supplier is an individual or a company that provides Glimepiride active pharmaceutical ingredient (API) or Glimepiride finished formulations upon request. The Glimepiride suppliers may include Glimepiride API manufacturers, exporters, distributors and traders.
click here to find a list of Glimepiride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glimepiride CEP of the European Pharmacopoeia monograph is often referred to as a Glimepiride Certificate of Suitability (COS). The purpose of a Glimepiride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Glimepiride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Glimepiride to their clients by showing that a Glimepiride CEP has been issued for it. The manufacturer submits a Glimepiride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Glimepiride CEP holder for the record. Additionally, the data presented in the Glimepiride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Glimepiride DMF.
A Glimepiride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Glimepiride 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 Glimepiride suppliers with CEP (COS) on PharmaCompass.
We have 20 companies offering Glimepiride
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