01 1Alivus Life Sciences
02 1Alkem Laboratories
03 1Apotex Pharmachem
04 1Esteve Quimica
05 1Hetero Drugs
06 1ScinoPharm Taiwan Ltd
07 1Standard Chem. & Pharm. Co., Ltd
08 1Sun Pharmaceutical Industries Limited
01 3RILUZOLE
02 5RILUZOLE USP
01 1Canada
02 4India
03 1Spain
04 2Taiwan
01 6Active
02 2Inactive
01 2Complete
02 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22107
Submission : 2008-10-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25260
Submission : 2011-09-24
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22596
Submission : 2009-03-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24693
Submission : 2011-02-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23215
Submission : 2009-10-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2023-02-23
Pay. Date : 2021-10-28
DMF Number : 15252
Submission : 2001-01-16
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-02-07
Pay. Date : 2013-04-08
DMF Number : 26147
Submission : 2012-06-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22438
Submission : 2009-03-16
Status : Active
Type : II
34
PharmaCompass offers a list of Riluzole API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Riluzole manufacturer or Riluzole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Riluzole manufacturer or Riluzole supplier.
A A13951 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of A13951, including repackagers and relabelers. The FDA regulates A13951 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. A13951 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of A13951 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A A13951 supplier is an individual or a company that provides A13951 active pharmaceutical ingredient (API) or A13951 finished formulations upon request. The A13951 suppliers may include A13951 API manufacturers, exporters, distributors and traders.
click here to find a list of A13951 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A A13951 DMF (Drug Master File) is a document detailing the whole manufacturing process of A13951 active pharmaceutical ingredient (API) in detail. Different forms of A13951 DMFs exist exist since differing nations have different regulations, such as A13951 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A A13951 DMF submitted to regulatory agencies in the US is known as a USDMF. A13951 USDMF includes data on A13951's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The A13951 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of A13951 suppliers with USDMF on PharmaCompass.
We have 7 companies offering A13951
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