Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 2COHANCE LIFESCIENCES LIMITED Mumbai IN
02 1SCI PHARMTECH, INC. Taoyuan City TW
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1HETERO LABS LIMITED Hyderabad IN
05 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
06 1MSN ORGANICS PRIVATE LIMITED Bibinagar Village IN
07 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
08 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : CEP 2015-150 - Rev 01
Status : Valid
Issue Date : 2024-07-09
Type : Chemical
Substance Number : 2640
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Certificate Number : CEP 2017-029 - Rev 04
Status : Valid
Issue Date : 2024-12-12
Type : Chemical
Substance Number : 2640
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Atomoxetine Hydrochloride, Process 2
Certificate Number : CEP 2019-212 - Rev 02
Status : Valid
Issue Date : 2024-07-10
Type : Chemical
Substance Number : 2640
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PharmaCompass offers a list of Atomoxetin Hydrochloride 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 Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Atomoxetin Hydrochloride API Price utilized in the formulation of products. Atomoxetin Hydrochloride API Price is not always fixed or binding as the Atomoxetin Hydrochloride Price is obtained through a variety of data sources. The Atomoxetin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LY 139603 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LY 139603, including repackagers and relabelers. The FDA regulates LY 139603 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LY 139603 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 LY 139603 supplier is an individual or a company that provides LY 139603 active pharmaceutical ingredient (API) or LY 139603 finished formulations upon request. The LY 139603 suppliers may include LY 139603 API manufacturers, exporters, distributors and traders.
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A LY 139603 CEP of the European Pharmacopoeia monograph is often referred to as a LY 139603 Certificate of Suitability (COS). The purpose of a LY 139603 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of LY 139603 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of LY 139603 to their clients by showing that a LY 139603 CEP has been issued for it. The manufacturer submits a LY 139603 CEP (COS) as part of the market authorization procedure, and it takes on the role of a LY 139603 CEP holder for the record. Additionally, the data presented in the LY 139603 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the LY 139603 DMF.
A LY 139603 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. LY 139603 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 LY 139603 suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering LY 139603
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