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 1Cayman Chemical Company Inc
05 1Gentec Pharmaceutical Group
06 1TAPI Technology & API Services
07 1C-Squared Pharma
08 1DELTA BIOTECH SA
09 1Everlight Chemical
10 1FDC
11 1FineTech Pharmaceutical Ltd.
12 1Industriale Chimica
13 1Kyowa Pharma Chemical Co Ltd
14 1Lupin Ltd
15 1MSN Laboratories
16 1NEWCHEM SPA
17 1Patheon
18 1Resolution Chemicals Limited
19 1Sai Life Sciences Limited
20 1Viatris
21 1Yonsung Fine Chemicals
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
GDUFA
DMF Review : Complete
Rev. Date : 2017-03-17
Pay. Date : 2016-11-10
DMF Number : 26081
Submission : 2012-05-14
Status :
Type : II
Chirogate is a professional Prostaglandin manufacturer.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18343
Submission : 2005-05-24
Status :
Type : II
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-11
Pay. Date : 2013-01-16
DMF Number : 26728
Submission : 2012-12-14
Status :
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-10
Pay. Date : 2013-08-16
DMF Number : 17445
Submission : 2004-06-01
Status :
Type : II
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
GDUFA
DMF Review : Complete
Rev. Date : 2021-10-15
Pay. Date : 2021-06-29
DMF Number : 34369
Submission : 2020-01-27
Status :
Type : II
TAPI offers customized CDMO Solutions for API development and manufacturing services.
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-26
Pay. Date : 2012-12-03
DMF Number : 22198
Submission : 2008-11-14
Status :
Type : II
Chirogate is a professional Prostaglandin manufacturer.
GDUFA
DMF Review : Complete
Rev. Date : 2017-04-13
Pay. Date : 2017-02-21
DMF Number : 31372
Submission : 2017-03-14
Status :
Type : II
A Latanoprost manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Latanoprost, including repackagers and relabelers. The FDA regulates Latanoprost manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Latanoprost 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 Latanoprost manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Latanoprost supplier is an individual or a company that provides Latanoprost active pharmaceutical ingredient (API) or Latanoprost finished formulations upon request. The Latanoprost suppliers may include Latanoprost API manufacturers, exporters, distributors and traders.
click here to find a list of Latanoprost suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Latanoprost DMF (Drug Master File) is a document detailing the whole manufacturing process of Latanoprost active pharmaceutical ingredient (API) in detail. Different forms of Latanoprost DMFs exist exist since differing nations have different regulations, such as Latanoprost USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Latanoprost DMF submitted to regulatory agencies in the US is known as a USDMF. Latanoprost USDMF includes data on Latanoprost's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Latanoprost USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Latanoprost suppliers with USDMF on PharmaCompass.
We have 21 companies offering Latanoprost
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
