Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Polpharma
02 1Biophore India Pharmaceuticals Pvt Ltd
03 1TAPI Technology & API Services
04 1Honour Lab Limited
05 1Alembic Pharmaceuticals Limited
06 1Aurobindo Pharma Limited
07 1Beijing Hope Pharmaceutical
08 1Cipla
09 1Jubilant Generics
10 1Lupin Ltd
11 1MSN Laboratories
12 1Macleods Pharmaceuticals Limited
13 1Morepen Laboratories
14 1Raks Pharma
15 1ScinoPharm Taiwan Ltd
16 1Signa S.A. de C.V.
17 1TOPHARMAN SHANDONG CO LTD
18 1Unichem Laboratories Limited
19 1Zhejiang Guobang Pharmaceutical
20 1Zhejiang Huahai Pharmaceutical
21 1Zydus Lifesciences
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32347
Submission : 2017-12-21
Status :
Type : II
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Complete
Rev. Date : 2019-04-16
Pay. Date : 2019-03-22
DMF Number : 33704
Submission : 2019-03-20
Status :
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2019-03-18
Pay. Date : 2018-10-01
DMF Number : 33450
Submission : 2019-02-12
Status :
Type : II
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
GDUFA
DMF Review : Complete
Rev. Date : 2018-07-10
Pay. Date : 2018-03-27
DMF Number : 32532
Submission : 2018-06-04
Status :
Type : II
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PharmaCompass offers a list of Brexpiprazole 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 Brexpiprazole manufacturer or Brexpiprazole supplier for your needs.
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A AKOS025291100 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS025291100, including repackagers and relabelers. The FDA regulates AKOS025291100 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS025291100 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 AKOS025291100 supplier is an individual or a company that provides AKOS025291100 active pharmaceutical ingredient (API) or AKOS025291100 finished formulations upon request. The AKOS025291100 suppliers may include AKOS025291100 API manufacturers, exporters, distributors and traders.
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A AKOS025291100 DMF (Drug Master File) is a document detailing the whole manufacturing process of AKOS025291100 active pharmaceutical ingredient (API) in detail. Different forms of AKOS025291100 DMFs exist exist since differing nations have different regulations, such as AKOS025291100 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AKOS025291100 DMF submitted to regulatory agencies in the US is known as a USDMF. AKOS025291100 USDMF includes data on AKOS025291100's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AKOS025291100 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 21 companies offering AKOS025291100
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