Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s.r.o
02 2Chirogate International
03 1EUROAPI
04 1Dr. Reddy's Laboratories
05 1Gentec Pharmaceutical Group
06 1Biocon
07 1Curia
08 1DELTA BIOTECH SA
09 1Everlight Chemical
10 1FineTech Pharmaceutical Ltd.
11 1IRIX Manufacturing Inc.
12 1Lupin Ltd
13 1MSN Laboratories
14 1ScinoPharm Taiwan Ltd
15 1Yonsung Fine Chemicals
16 1Zhejiang Ausun Pharmaceutical
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-27
Pay. Date : 2013-02-08
DMF Number : 22289
Submission : 2008-12-08
Status :
Type : II
Chirogate is a professional Prostaglandin manufacturer.
GDUFA
DMF Review : Complete
Rev. Date : 2012-11-23
Pay. Date : 2012-12-17
DMF Number : 22738
Submission : 2009-04-20
Status :
Type : II
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34742
Submission : 2020-12-24
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14890
Submission : 2000-05-08
Status :
Type : II
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34370
Submission : 2020-01-27
Status :
Type : II
Chirogate is a professional Prostaglandin manufacturer.
GDUFA
DMF Review : Complete
Rev. Date : 2022-03-01
Pay. Date : 2022-01-05
DMF Number : 32964
Submission : 2018-07-27
Status :
Type : II
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PharmaCompass offers a list of Travoprost 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 Travoprost manufacturer or Travoprost supplier for your needs.
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A IZBA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of IZBA, including repackagers and relabelers. The FDA regulates IZBA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. IZBA 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 IZBA supplier is an individual or a company that provides IZBA active pharmaceutical ingredient (API) or IZBA finished formulations upon request. The IZBA suppliers may include IZBA API manufacturers, exporters, distributors and traders.
click here to find a list of IZBA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A IZBA DMF (Drug Master File) is a document detailing the whole manufacturing process of IZBA active pharmaceutical ingredient (API) in detail. Different forms of IZBA DMFs exist exist since differing nations have different regulations, such as IZBA USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A IZBA DMF submitted to regulatory agencies in the US is known as a USDMF. IZBA USDMF includes data on IZBA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The IZBA USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of IZBA suppliers with USDMF on PharmaCompass.
We have 16 companies offering IZBA
Get in contact with the supplier of your choice:
