01 1Tokuyama Corporation
02 2Blank
01 3PROPANTHELINE BROMIDE
01 1Japan
02 2Blank
01 3Inactive
01 3Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17140
Submission : 2004-02-06
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3603
Submission : 1979-09-11
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 : 2321
Submission : 1974-08-26
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Propantheline Bromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Propantheline Bromide manufacturer or Propantheline Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propantheline Bromide manufacturer or Propantheline Bromide supplier.
A Ketaman manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketaman, including repackagers and relabelers. The FDA regulates Ketaman manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketaman 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 Ketaman manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ketaman supplier is an individual or a company that provides Ketaman active pharmaceutical ingredient (API) or Ketaman finished formulations upon request. The Ketaman suppliers may include Ketaman API manufacturers, exporters, distributors and traders.
click here to find a list of Ketaman suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Ketaman DMF (Drug Master File) is a document detailing the whole manufacturing process of Ketaman active pharmaceutical ingredient (API) in detail. Different forms of Ketaman DMFs exist exist since differing nations have different regulations, such as Ketaman USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ketaman DMF submitted to regulatory agencies in the US is known as a USDMF. Ketaman USDMF includes data on Ketaman's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ketaman USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ketaman suppliers with USDMF on PharmaCompass.
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