PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
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01 1PMC Isochem
02 3Hainan Poly Pharm
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01 1TRIMEBUTINE MALEATE
02 2TRIMEBUTINE MALEATE DRUG SUBSTANCE
03 1TRIMEBUTINE MALEATE TABLETS
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01 3China
02 1France
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01 2Active
02 2Inactive
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01 4Blank
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19765
Submission : 2006-09-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34948
Submission : 2020-06-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23725
Submission : 2010-04-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24203
Submission : 2010-08-26
Status : Inactive
Type : II
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PharmaCompass offers a list of Trimebutine Maleate 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 Trimebutine Maleate manufacturer or Trimebutine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trimebutine Maleate manufacturer or Trimebutine Maleate supplier.
PharmaCompass also assists you with knowing the Trimebutine Maleate API Price utilized in the formulation of products. Trimebutine Maleate API Price is not always fixed or binding as the Trimebutine Maleate Price is obtained through a variety of data sources. The Trimebutine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Debridat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Debridat, including repackagers and relabelers. The FDA regulates Debridat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Debridat 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 Debridat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Debridat supplier is an individual or a company that provides Debridat active pharmaceutical ingredient (API) or Debridat finished formulations upon request. The Debridat suppliers may include Debridat API manufacturers, exporters, distributors and traders.
click here to find a list of Debridat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Debridat DMF (Drug Master File) is a document detailing the whole manufacturing process of Debridat active pharmaceutical ingredient (API) in detail. Different forms of Debridat DMFs exist exist since differing nations have different regulations, such as Debridat USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Debridat DMF submitted to regulatory agencies in the US is known as a USDMF. Debridat USDMF includes data on Debridat's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Debridat USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Debridat suppliers with USDMF on PharmaCompass.
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