Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 1DISHMAN NETHERLANDS B.V.
03 1Massachusetts General Hospital
01 11 ALPHA-HYDROXYDIHYDROTACHYSTEROL 3
02 2DIHYDROTACHYSTEROL
01 1France
02 1Netherlands
03 1U.S.A
01 1Active
02 2Inactive
01 3Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5730
Submission : 1985-03-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4691
Submission : 1982-10-19
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3317
Submission : 1978-10-06
Status : Inactive
Type : II
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PharmaCompass offers a list of Dihydrotachysterol 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 Dihydrotachysterol manufacturer or Dihydrotachysterol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dihydrotachysterol manufacturer or Dihydrotachysterol supplier.
PharmaCompass also assists you with knowing the Dihydrotachysterol API Price utilized in the formulation of products. Dihydrotachysterol API Price is not always fixed or binding as the Dihydrotachysterol Price is obtained through a variety of data sources. The Dihydrotachysterol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dihydrotachysterol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dihydrotachysterol, including repackagers and relabelers. The FDA regulates Dihydrotachysterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dihydrotachysterol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Dihydrotachysterol supplier is an individual or a company that provides Dihydrotachysterol active pharmaceutical ingredient (API) or Dihydrotachysterol finished formulations upon request. The Dihydrotachysterol suppliers may include Dihydrotachysterol API manufacturers, exporters, distributors and traders.
click here to find a list of Dihydrotachysterol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dihydrotachysterol DMF (Drug Master File) is a document detailing the whole manufacturing process of Dihydrotachysterol active pharmaceutical ingredient (API) in detail. Different forms of Dihydrotachysterol DMFs exist exist since differing nations have different regulations, such as Dihydrotachysterol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dihydrotachysterol DMF submitted to regulatory agencies in the US is known as a USDMF. Dihydrotachysterol USDMF includes data on Dihydrotachysterol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dihydrotachysterol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dihydrotachysterol suppliers with USDMF on PharmaCompass.
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