EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 1Supriya Lifescience
03 1Blank
01 1HYDROXOCOBALAMIN
02 1HYDROXOCOBALAMIN BASE
03 1HYDROXOCOBALAMIN USP
01 1France
02 1India
03 1Blank
01 2Active
02 1Inactive
01 3Blank
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18216
Submission : 2005-03-30
Status : Active
Type : II
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37168
Submission : 2022-06-04
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9100
Submission : 1991-05-06
Status : Inactive
Type : II
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PharmaCompass offers a list of Hydroxocobalamin 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 Hydroxocobalamin manufacturer or Hydroxocobalamin supplier for your needs.
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A Cyanokit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyanokit, including repackagers and relabelers. The FDA regulates Cyanokit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyanokit 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 Cyanokit supplier is an individual or a company that provides Cyanokit active pharmaceutical ingredient (API) or Cyanokit finished formulations upon request. The Cyanokit suppliers may include Cyanokit API manufacturers, exporters, distributors and traders.
click here to find a list of Cyanokit suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cyanokit DMF (Drug Master File) is a document detailing the whole manufacturing process of Cyanokit active pharmaceutical ingredient (API) in detail. Different forms of Cyanokit DMFs exist exist since differing nations have different regulations, such as Cyanokit USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cyanokit DMF submitted to regulatory agencies in the US is known as a USDMF. Cyanokit USDMF includes data on Cyanokit's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cyanokit USDMF is kept confidential to protect the manufacturer’s intellectual property.
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