01 1Catalytica
02 1Esteve Quimica
03 1Johnson & Johnson Innovative Medicine
04 1Quimica Sintetica
05 2Blank
01 4ASTEMIZOLE
02 1ASTEMIZOLE INTERMEDIATES
03 1ASTEMIZOLE-R 43512
01 1India
02 2Spain
03 1U.S.A
04 2Blank
01 6Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10889
Submission : 1994-05-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11584
Submission : 1995-07-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5172
Submission : 1983-11-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9443
Submission : 1991-11-11
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8510
Submission : 1990-04-04
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9599
Submission : 1992-03-04
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
65
PharmaCompass offers a list of Astemizole 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 Astemizole manufacturer or Astemizole supplier for your needs.
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PharmaCompass also assists you with knowing the Astemizole API Price utilized in the formulation of products. Astemizole API Price is not always fixed or binding as the Astemizole Price is obtained through a variety of data sources. The Astemizole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nono-Nastizol A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nono-Nastizol A, including repackagers and relabelers. The FDA regulates Nono-Nastizol A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nono-Nastizol A 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 Nono-Nastizol A supplier is an individual or a company that provides Nono-Nastizol A active pharmaceutical ingredient (API) or Nono-Nastizol A finished formulations upon request. The Nono-Nastizol A suppliers may include Nono-Nastizol A API manufacturers, exporters, distributors and traders.
click here to find a list of Nono-Nastizol A suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Nono-Nastizol A DMF (Drug Master File) is a document detailing the whole manufacturing process of Nono-Nastizol A active pharmaceutical ingredient (API) in detail. Different forms of Nono-Nastizol A DMFs exist exist since differing nations have different regulations, such as Nono-Nastizol A USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Nono-Nastizol A DMF submitted to regulatory agencies in the US is known as a USDMF. Nono-Nastizol A USDMF includes data on Nono-Nastizol A's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Nono-Nastizol A USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 4 companies offering Nono-Nastizol A
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