01 1Yamasa Corporation
02 1Yuki Gosei Kogyo
01 12' DEOXYCYTIDINE HYDROCHLORIDE (BULK)
02 12'-DEOXYCYTIDINE HYDROCHLORIDE
01 2Japan
01 2Inactive
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11943
Submission : 1996-04-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7268
Submission : 1987-12-12
Status : Inactive
Type : II
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PharmaCompass offers a list of Deoxycytidine Hydrochloride 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 Deoxycytidine Hydrochloride manufacturer or Deoxycytidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Deoxycytidine Hydrochloride manufacturer or Deoxycytidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Deoxycytidine Hydrochloride API Price utilized in the formulation of products. Deoxycytidine Hydrochloride API Price is not always fixed or binding as the Deoxycytidine Hydrochloride Price is obtained through a variety of data sources. The Deoxycytidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deoxycytidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deoxycytidine Hydrochloride, including repackagers and relabelers. The FDA regulates Deoxycytidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deoxycytidine Hydrochloride 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 Deoxycytidine Hydrochloride supplier is an individual or a company that provides Deoxycytidine Hydrochloride active pharmaceutical ingredient (API) or Deoxycytidine Hydrochloride finished formulations upon request. The Deoxycytidine Hydrochloride suppliers may include Deoxycytidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Deoxycytidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Deoxycytidine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Deoxycytidine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Deoxycytidine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Deoxycytidine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Deoxycytidine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Deoxycytidine Hydrochloride USDMF includes data on Deoxycytidine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Deoxycytidine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Deoxycytidine Hydrochloride suppliers with USDMF on PharmaCompass.
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