01 1AMINO GmbH
02 2Ajinomoto Company
03 1Kyowa Hakko Bio
04 2Mitsubishi Tanabe Pharma
05 1Nippon Kayaku
06 1SIGMA TAU
01 7L-ISOLEUCINE
02 1L-THREONINE, L-TRYTOPHAN & L-ISOLEUCINE
01 1Germany
02 6Japan
03 1U.S.A
01 3Active
02 5Inactive
01 2Complete
02 6Blank
GDUFA
DMF Review : Complete
Rev. Date : 2017-05-12
Pay. Date : 2017-04-17
DMF Number : 29143
Submission : 2015-02-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-08-14
Pay. Date : 2018-07-05
DMF Number : 21991
Submission : 2008-07-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4041
Submission : 1980-10-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2623
Submission : 1976-02-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1250
Submission : 1968-10-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9422
Submission : 1991-11-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4822
Submission : 1982-12-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9991
Submission : 1992-11-25
Status : Inactive
Type : II
33
PharmaCompass offers a list of Isoleucine 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 Isoleucine manufacturer or Isoleucine supplier for your needs.
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A 04Y7590D77 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04Y7590D77, including repackagers and relabelers. The FDA regulates 04Y7590D77 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04Y7590D77 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 04Y7590D77 DMF (Drug Master File) is a document detailing the whole manufacturing process of 04Y7590D77 active pharmaceutical ingredient (API) in detail. Different forms of 04Y7590D77 DMFs exist exist since differing nations have different regulations, such as 04Y7590D77 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
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