01 2Bayer AG
02 1Olon S.p.A
03 2Blank
01 1BAYER 2353 (YOMESAN)
02 2NICLOSAMIDE
03 1NICLOSAMIDE 500MG TABLET
04 1NICLOSAMIDE ANHYDROUS DRUG SUBSTANCE
01 2Germany
02 1Italy
03 2Blank
01 1Active
02 4Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25273
Submission : 2011-10-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25274
Submission : 2011-10-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34597
Submission : 2020-02-13
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4146
Submission : 1981-01-31
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 : 557
Submission : 1963-05-20
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
84
PharmaCompass offers a list of Niclosamide 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 Niclosamide manufacturer or Niclosamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Niclosamide manufacturer or Niclosamide supplier.
PharmaCompass also assists you with knowing the Niclosamide API Price utilized in the formulation of products. Niclosamide API Price is not always fixed or binding as the Niclosamide Price is obtained through a variety of data sources. The Niclosamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Devermin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Devermin, including repackagers and relabelers. The FDA regulates Devermin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Devermin 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 Devermin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Devermin supplier is an individual or a company that provides Devermin active pharmaceutical ingredient (API) or Devermin finished formulations upon request. The Devermin suppliers may include Devermin API manufacturers, exporters, distributors and traders.
click here to find a list of Devermin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Devermin DMF (Drug Master File) is a document detailing the whole manufacturing process of Devermin active pharmaceutical ingredient (API) in detail. Different forms of Devermin DMFs exist exist since differing nations have different regulations, such as Devermin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Devermin DMF submitted to regulatory agencies in the US is known as a USDMF. Devermin USDMF includes data on Devermin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Devermin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Devermin suppliers with USDMF on PharmaCompass.
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