01 4Fujifilm Diosynth Biotechnologies
02 1SAFC
03 1SIGMA TAU
01 1BOVINE INSULIN
02 2BOVINE INSULIN HIGHLY PURIFIED
03 1BOVINE INSULINE HIGHLY PURIFIED
04 1INSULIN FROM BOVINE PANCREAS
05 1TrypZean Bovine, Recombinant Expressed in Corn
01 2U.S.A
02 4United Kingdom
01 6Inactive
01 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14833
Submission : 2000-04-14
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14382
Submission : 1999-09-02
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3881
Submission : 1980-06-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3865
Submission : 1980-06-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21228
Submission : 2008-01-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7679
Submission : 1988-09-15
Status : Inactive
Type : II
16
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A VELOSULIN BR HUMAN DMF (Drug Master File) is a document detailing the whole manufacturing process of VELOSULIN BR HUMAN active pharmaceutical ingredient (API) in detail. Different forms of VELOSULIN BR HUMAN DMFs exist exist since differing nations have different regulations, such as VELOSULIN BR HUMAN USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A VELOSULIN BR HUMAN DMF submitted to regulatory agencies in the US is known as a USDMF. VELOSULIN BR HUMAN USDMF includes data on VELOSULIN BR HUMAN's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The VELOSULIN BR HUMAN USDMF is kept confidential to protect the manufacturer’s intellectual property.
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