EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 1TAPI Technology & API Services
03 1Apicore LLC
04 1Catalent Pharma Solutions
05 2Catalytica
06 1DMFs Not Supported
07 2Dipharma
08 1Resolution Chemicals Limited
09 3Siegfried AG
10 1Trifarma
11 1Viatris
12 2Blank
01 1R-NORSELEGILINE BASE AND HYDROCHLORIDE
02 1SELEGIINE
03 3SELEGILINE
04 1SELEGILINE (DEPRENYL) HYDROCHLORIDE
05 1SELEGILINE BASE
06 9SELEGILINE HYDROCHLORIDE
07 1SELEGILINE HYDROCHLORIDE ZYDIS TABLET 1.25MG
01 1France
02 3India
03 1Israel
04 3Italy
05 3Switzerland
06 2U.S.A
07 1United Kingdom
08 3Blank
01 6Active
02 11Inactive
01 2Complete
02 15Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5161
Submission : 1983-12-01
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10235
Submission : 1993-05-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37046
Submission : 2022-05-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15914
Submission : 2002-03-27
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9230
Submission : 1991-07-10
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-10-05
Pay. Date : 2017-07-25
DMF Number : 30957
Submission : 2017-06-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-02-07
Pay. Date : 2014-02-03
DMF Number : 9275
Submission : 1991-08-05
Status : Active
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10036
Submission : 1992-12-30
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9734
Submission : 1992-06-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38797
Submission : 2023-09-27
Status : Active
Type : II
A Selegiline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selegiline, including repackagers and relabelers. The FDA regulates Selegiline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selegiline 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 Selegiline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selegiline supplier is an individual or a company that provides Selegiline active pharmaceutical ingredient (API) or Selegiline finished formulations upon request. The Selegiline suppliers may include Selegiline API manufacturers, exporters, distributors and traders.
click here to find a list of Selegiline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selegiline DMF (Drug Master File) is a document detailing the whole manufacturing process of Selegiline active pharmaceutical ingredient (API) in detail. Different forms of Selegiline DMFs exist exist since differing nations have different regulations, such as Selegiline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Selegiline DMF submitted to regulatory agencies in the US is known as a USDMF. Selegiline USDMF includes data on Selegiline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Selegiline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Selegiline suppliers with USDMF on PharmaCompass.
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