Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s.r.o
02 1Chirogate International
03 1ASAHI GLASS CO LTD
04 1Everlight Chemical
05 1MSN Laboratories
06 1Zhejiang Ausun Pharmaceutical
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
GDUFA
DMF Review : Complete
Rev. Date : 2021-07-15
Pay. Date : 2021-04-06
DMF Number : 35765
Submission : 2021-04-12
Status :
Type : II
Chirogate is a professional Prostaglandin manufacturer.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33632
Submission : 2019-04-11
Status :
Type : II
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PharmaCompass offers a list of Tafluprost 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 Tafluprost manufacturer or Tafluprost supplier for your needs.
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A Zioptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zioptan, including repackagers and relabelers. The FDA regulates Zioptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zioptan 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 Zioptan supplier is an individual or a company that provides Zioptan active pharmaceutical ingredient (API) or Zioptan finished formulations upon request. The Zioptan suppliers may include Zioptan API manufacturers, exporters, distributors and traders.
click here to find a list of Zioptan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zioptan DMF (Drug Master File) is a document detailing the whole manufacturing process of Zioptan active pharmaceutical ingredient (API) in detail. Different forms of Zioptan DMFs exist exist since differing nations have different regulations, such as Zioptan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zioptan DMF submitted to regulatory agencies in the US is known as a USDMF. Zioptan USDMF includes data on Zioptan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zioptan USDMF is kept confidential to protect the manufacturer’s intellectual property.
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