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01 1Catalytica
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01 1BUTAMBEN USP
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01 1India
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01 1Inactive
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01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11781
Submission : 1995-12-19
Status : Inactive
Type : II
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PharmaCompass offers a list of Butamben 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 Butamben manufacturer or Butamben supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Butamben manufacturer or Butamben supplier.
PharmaCompass also assists you with knowing the Butamben API Price utilized in the formulation of products. Butamben API Price is not always fixed or binding as the Butamben Price is obtained through a variety of data sources. The Butamben Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Butoforme manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Butoforme, including repackagers and relabelers. The FDA regulates Butoforme manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Butoforme 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 Butoforme manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Butoforme supplier is an individual or a company that provides Butoforme active pharmaceutical ingredient (API) or Butoforme finished formulations upon request. The Butoforme suppliers may include Butoforme API manufacturers, exporters, distributors and traders.
click here to find a list of Butoforme suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Butoforme DMF (Drug Master File) is a document detailing the whole manufacturing process of Butoforme active pharmaceutical ingredient (API) in detail. Different forms of Butoforme DMFs exist exist since differing nations have different regulations, such as Butoforme USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Butoforme DMF submitted to regulatory agencies in the US is known as a USDMF. Butoforme USDMF includes data on Butoforme's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Butoforme USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Butoforme suppliers with USDMF on PharmaCompass.