01 1Fujifilm Diosynth Biotechnologies
02 2Monachem Specialities
03 1NEWCHEM SPA
04 2Sterling Spa
05 1Teva Pharmaceutical Industries
01 1GRADE B NOMAC
02 3NOMEGESTROL ACETATE
03 1NOMEGESTROL ACETATE CODE 204622
04 1NOMEGESTROL ACETATE, NOMAC GRADE B
05 1NOMEGESTROL ACTATE
01 2India
02 1Israel
03 3Italy
04 1United Kingdom
01 4Active
02 3Inactive
01 7Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9232
Submission : 1991-08-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17534
Submission : 2004-07-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13987
Submission : 1999-02-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22750
Submission : 2009-04-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28125
Submission : 2014-03-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23921
Submission : 2010-06-25
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36055
Submission : 2021-06-25
Status : Active
Type : II
54
PharmaCompass offers a list of Nomegestrol Acetate 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 Nomegestrol Acetate manufacturer or Nomegestrol Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Nomegestrol Acetate API Price utilized in the formulation of products. Nomegestrol Acetate API Price is not always fixed or binding as the Nomegestrol Acetate Price is obtained through a variety of data sources. The Nomegestrol Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutenyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutenyl, including repackagers and relabelers. The FDA regulates Lutenyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutenyl 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 Lutenyl supplier is an individual or a company that provides Lutenyl active pharmaceutical ingredient (API) or Lutenyl finished formulations upon request. The Lutenyl suppliers may include Lutenyl API manufacturers, exporters, distributors and traders.
click here to find a list of Lutenyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lutenyl DMF (Drug Master File) is a document detailing the whole manufacturing process of Lutenyl active pharmaceutical ingredient (API) in detail. Different forms of Lutenyl DMFs exist exist since differing nations have different regulations, such as Lutenyl USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lutenyl DMF submitted to regulatory agencies in the US is known as a USDMF. Lutenyl USDMF includes data on Lutenyl's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lutenyl USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lutenyl suppliers with USDMF on PharmaCompass.
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