01 1CHEMSYN CHEMICAL CORPORATION
02 1F. Hoffmann-La Roche
01 1ALTRETAMINE
02 1HEXASTAT CAPS, 50 & 100MG
01 1Canada
02 1Switzerland
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9703
Submission : 1992-05-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4412
Submission : 1981-12-18
Status : Inactive
Type : II
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PharmaCompass offers a list of Altretamine 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 Altretamine manufacturer or Altretamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Altretamine manufacturer or Altretamine supplier.
PharmaCompass also assists you with knowing the Altretamine API Price utilized in the formulation of products. Altretamine API Price is not always fixed or binding as the Altretamine Price is obtained through a variety of data sources. The Altretamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hexalen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hexalen, including repackagers and relabelers. The FDA regulates Hexalen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hexalen API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Hexalen supplier is an individual or a company that provides Hexalen active pharmaceutical ingredient (API) or Hexalen finished formulations upon request. The Hexalen suppliers may include Hexalen API manufacturers, exporters, distributors and traders.
click here to find a list of Hexalen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hexalen DMF (Drug Master File) is a document detailing the whole manufacturing process of Hexalen active pharmaceutical ingredient (API) in detail. Different forms of Hexalen DMFs exist exist since differing nations have different regulations, such as Hexalen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hexalen DMF submitted to regulatory agencies in the US is known as a USDMF. Hexalen USDMF includes data on Hexalen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hexalen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hexalen suppliers with USDMF on PharmaCompass.
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