01 1Apicore
02 1Emcure Pharmaceuticals
03 1Jubilant Generics
04 1Macleods Pharmaceuticals Limited
05 1Trifarma
01 1PERPHENAZINE
02 4PERPHENAZINE USP
01 4India
02 1Italy
01 5Active
01 5Complete
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-27
Pay. Date : 2012-11-28
DMF Number : 24646
Submission : 2012-11-28
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-06
Pay. Date : 2014-01-22
DMF Number : 27224
Submission : 2013-06-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-09-16
Pay. Date : 2019-08-22
DMF Number : 31379
Submission : 2017-03-29
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-12-27
Pay. Date : 2016-09-28
DMF Number : 30756
Submission : 2016-09-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-15
Pay. Date : 2012-12-19
DMF Number : 4130
Submission : 1981-02-27
Status : Active
Type : II
57
PharmaCompass offers a list of Perphenazine 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 Perphenazine manufacturer or Perphenazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Perphenazine manufacturer or Perphenazine supplier.
PharmaCompass also assists you with knowing the Perphenazine API Price utilized in the formulation of products. Perphenazine API Price is not always fixed or binding as the Perphenazine Price is obtained through a variety of data sources. The Perphenazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EU-0100930 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EU-0100930, including repackagers and relabelers. The FDA regulates EU-0100930 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EU-0100930 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 EU-0100930 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EU-0100930 supplier is an individual or a company that provides EU-0100930 active pharmaceutical ingredient (API) or EU-0100930 finished formulations upon request. The EU-0100930 suppliers may include EU-0100930 API manufacturers, exporters, distributors and traders.
click here to find a list of EU-0100930 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EU-0100930 DMF (Drug Master File) is a document detailing the whole manufacturing process of EU-0100930 active pharmaceutical ingredient (API) in detail. Different forms of EU-0100930 DMFs exist exist since differing nations have different regulations, such as EU-0100930 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A EU-0100930 DMF submitted to regulatory agencies in the US is known as a USDMF. EU-0100930 USDMF includes data on EU-0100930's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The EU-0100930 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of EU-0100930 suppliers with USDMF on PharmaCompass.
We have 5 companies offering EU-0100930
Get in contact with the supplier of your choice:
