Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1COHANCE LIFESCIENCES LIMITED Mumbai IN
02 1EGIS Pharmaceuticals PLC Budapest HU
03 1NEULAND LABORATORIES LIMITED Hyderabad IN
04 1TAPI NL B.V. Amsterdam NL
05 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
06 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
07 3AUROBINDO PHARMA LIMITED Hyderabad IN
08 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
09 1DÜLLBERG KONZENTRA GMBH & CO. KG Hamburg DE
10 2HETERO LABS LIMITED Hyderabad IN
11 1JUBILANT BIOSYS LIMITED Nanjangud IN
12 2MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
13 1MATRIX PHARMACORP PRIVATE LIMITED Sangareddy District IN
14 1MSN PHARMACHEM PRIVATE LIMITED Sangareddy District IN
15 1NIFTY LABS PRIVATE LIMITED Hyderabad IN
16 1OLON S.P.A. Rodano IT
17 1PHARMACEUTICAL SOLUTIONS FZCO Dubai AE
18 1RUYUAN HEC PHARM CO., LTD. Shaoguan CN
19 1SCHWABE EXTRACTA GMBH & CO. KG Karlsruhe DE
20 1SMS PHARMACEUTICALS LIMITED Hyderabad IN
21 1SYNTHON B.V. Nijmegen NL
22 1UNICHEM LABORATORIES LIMITED Mumbai IN
23 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
24 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 2016-021 - Rev 02
Status : Valid
Issue Date : 2024-07-09
Type : Chemical
Substance Number : 2617
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 2014-252 - Rev 02
Status : Valid
Issue Date : 2022-07-21
Type : Chemical
Substance Number : 2617
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : CEP 2017-289 - Rev 03
Status : Valid
Issue Date : 2024-04-25
Type : Chemical
Substance Number : 2617
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2018-267 - Rev 03
Status : Valid
Issue Date : 2025-06-05
Type : Chemical
Substance Number : 2617
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PharmaCompass offers a list of Aripiprazole 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 Aripiprazole manufacturer or Aripiprazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aripiprazole manufacturer or Aripiprazole supplier.
PharmaCompass also assists you with knowing the Aripiprazole API Price utilized in the formulation of products. Aripiprazole API Price is not always fixed or binding as the Aripiprazole Price is obtained through a variety of data sources. The Aripiprazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DL-178 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DL-178, including repackagers and relabelers. The FDA regulates DL-178 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DL-178 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 DL-178 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DL-178 supplier is an individual or a company that provides DL-178 active pharmaceutical ingredient (API) or DL-178 finished formulations upon request. The DL-178 suppliers may include DL-178 API manufacturers, exporters, distributors and traders.
click here to find a list of DL-178 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DL-178 CEP of the European Pharmacopoeia monograph is often referred to as a DL-178 Certificate of Suitability (COS). The purpose of a DL-178 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DL-178 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DL-178 to their clients by showing that a DL-178 CEP has been issued for it. The manufacturer submits a DL-178 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DL-178 CEP holder for the record. Additionally, the data presented in the DL-178 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DL-178 DMF.
A DL-178 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DL-178 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 DL-178 suppliers with CEP (COS) on PharmaCompass.
We have 23 companies offering DL-178
Get in contact with the supplier of your choice:
