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 1Inke S.A
04 1EUROAPI
05 1Cayman Chemical Company Inc
06 1C-Squared Pharma
07 1DELTA BIOTECH SA
08 1Everlight Chemical
09 1FDC
10 1FineTech Pharmaceutical Ltd.
11 1Industriale Chimica
12 1Kyowa Pharma Chemical Co Ltd
13 1Lupin Ltd
14 1MSN Laboratories
15 1NEWCHEM SPA
16 1Patheon
17 1Resolution Chemicals Limited
18 1Sai Life Sciences Limited
19 1Viatris
20 1Yonsung Fine Chemicals
21 1Zhejiang Ausun Pharmaceutical
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
Inke S.A: APIs manufacturing plant.
GDUFA
DMF Review : Complete
Rev. Date : 2021-10-15
Pay. Date : 2021-06-29
DMF Number : 34369
Submission : 2020-01-27
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
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
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A Iopize manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Iopize, including repackagers and relabelers. The FDA regulates Iopize manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Iopize 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 Iopize supplier is an individual or a company that provides Iopize active pharmaceutical ingredient (API) or Iopize finished formulations upon request. The Iopize suppliers may include Iopize API manufacturers, exporters, distributors and traders.
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A Iopize DMF (Drug Master File) is a document detailing the whole manufacturing process of Iopize active pharmaceutical ingredient (API) in detail. Different forms of Iopize DMFs exist exist since differing nations have different regulations, such as Iopize USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Iopize DMF submitted to regulatory agencies in the US is known as a USDMF. Iopize USDMF includes data on Iopize's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Iopize USDMF is kept confidential to protect the manufacturer’s intellectual property.
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