Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 2Sanofi
02 1Aspen API
03 2Bayer AG
04 1Fareva
05 2Gedeon Richter
06 1Lupin Ltd
07 1Merck & Co
08 1Mitsubishi Corporation
09 1Naari
10 1Zhejiang Xianju Junye Pharmaceutical Co. LTD
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01 7NORETHINDRONE
02 1NORETHINDRONE 1 MG. AND MESTRANOL 0.05 MG. TABLETS IN BULK
03 1NORETHINDRONE INJECTABLE MICROSPHERES - CINCINNATI, OHIO
04 1NORETHINDRONE USP
05 1NORETHINDRONE, BULK
06 3NORETHISTERONE
07 1NORTHINDRONE
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01 1China
02 2France
03 2Germany
04 2Hungary
05 2India
06 1Japan
07 1Luxembourg
08 1Netherlands
09 1U.S.A
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01 5Active
02 10Inactive
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01 3Complete
02 12Blank
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 : 1920
Submission : 1972-04-17
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-26
Pay. Date : 2012-11-20
DMF Number : 3849
Submission : 1980-05-22
Status : Active
Type : II
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 : 8239
Submission : 1989-10-05
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-05
Pay. Date : 2013-01-28
DMF Number : 2726
Submission : 1976-08-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2046
Submission : 1973-02-08
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-06-05
Pay. Date : 2013-09-18
DMF Number : 24416
Submission : 2011-03-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22505
Submission : 2009-02-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2010
Submission : 1972-10-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35803
Submission : 2021-03-30
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2068
Submission : 1973-01-29
Status : Inactive
Type : II
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PharmaCompass offers a list of Norethisterone 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 Norethisterone manufacturer or Norethisterone supplier for your needs.
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A Trinovum 21 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trinovum 21, including repackagers and relabelers. The FDA regulates Trinovum 21 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trinovum 21 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 Trinovum 21 supplier is an individual or a company that provides Trinovum 21 active pharmaceutical ingredient (API) or Trinovum 21 finished formulations upon request. The Trinovum 21 suppliers may include Trinovum 21 API manufacturers, exporters, distributors and traders.
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A Trinovum 21 DMF (Drug Master File) is a document detailing the whole manufacturing process of Trinovum 21 active pharmaceutical ingredient (API) in detail. Different forms of Trinovum 21 DMFs exist exist since differing nations have different regulations, such as Trinovum 21 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trinovum 21 DMF submitted to regulatory agencies in the US is known as a USDMF. Trinovum 21 USDMF includes data on Trinovum 21's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trinovum 21 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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