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 1Veranova
05 1Dr. Reddy's Laboratories
06 1Gentec Pharmaceutical Group
07 1Biocon
08 1Curia
09 1DELTA BIOTECH SA
10 1Everlight Chemical
11 1FineTech Pharmaceutical Ltd.
12 1IRIX Manufacturing Inc.
13 1Lupin Ltd
14 1MSN Laboratories
15 1ScinoPharm Taiwan, Ltd
16 1Yonsung Fine Chemicals
17 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
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22088
Submission : 2008-10-14
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
A Travoprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Travoprost, including repackagers and relabelers. The FDA regulates Travoprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Travoprost 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 Travoprost manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Travoprost supplier is an individual or a company that provides Travoprost active pharmaceutical ingredient (API) or Travoprost finished formulations upon request. The Travoprost suppliers may include Travoprost API manufacturers, exporters, distributors and traders.
click here to find a list of Travoprost suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Travoprost DMF (Drug Master File) is a document detailing the whole manufacturing process of Travoprost active pharmaceutical ingredient (API) in detail. Different forms of Travoprost DMFs exist exist since differing nations have different regulations, such as Travoprost USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Travoprost DMF submitted to regulatory agencies in the US is known as a USDMF. Travoprost USDMF includes data on Travoprost's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Travoprost USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Travoprost suppliers with USDMF on PharmaCompass.
We have 17 companies offering Travoprost
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