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01 1Unimark Remedies
02 1Johnson & Johnson Innovative Medicine
03 1Merck & Co
04 1Par Pharmaceutical
05 1Sai Life Sciences Limited
06 1Vasudha Pharma Chem
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01 2PIMOZIDE
02 3PIMOZIDE USP
03 1PIMOZIDE USP [TYPE-2]
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01 3India
02 3U.S.A
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01 3Active
02 3Inactive
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01 1Complete
02 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22747
Submission : 2009-04-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10872
Submission : 1994-04-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8426
Submission : 1990-02-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25462
Submission : 2011-12-14
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28495
Submission : 2014-10-31
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-03-11
Pay. Date : 2013-09-27
DMF Number : 27583
Submission : 2013-10-21
Status : Active
Type : II
21
PharmaCompass offers a list of Pimozide 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 Pimozide manufacturer or Pimozide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pimozide manufacturer or Pimozide supplier.
PharmaCompass also assists you with knowing the Pimozide API Price utilized in the formulation of products. Pimozide API Price is not always fixed or binding as the Pimozide Price is obtained through a variety of data sources. The Pimozide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NCGC00024888-03 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024888-03, including repackagers and relabelers. The FDA regulates NCGC00024888-03 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024888-03 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 NCGC00024888-03 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NCGC00024888-03 supplier is an individual or a company that provides NCGC00024888-03 active pharmaceutical ingredient (API) or NCGC00024888-03 finished formulations upon request. The NCGC00024888-03 suppliers may include NCGC00024888-03 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024888-03 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NCGC00024888-03 DMF (Drug Master File) is a document detailing the whole manufacturing process of NCGC00024888-03 active pharmaceutical ingredient (API) in detail. Different forms of NCGC00024888-03 DMFs exist exist since differing nations have different regulations, such as NCGC00024888-03 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NCGC00024888-03 DMF submitted to regulatory agencies in the US is known as a USDMF. NCGC00024888-03 USDMF includes data on NCGC00024888-03's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NCGC00024888-03 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NCGC00024888-03 suppliers with USDMF on PharmaCompass.
We have 6 companies offering NCGC00024888-03
Get in contact with the supplier of your choice: