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 Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selegiline Hydrochloride, including repackagers and relabelers. The FDA regulates Selegiline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selegiline Hydrochloride 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 Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selegiline Hydrochloride supplier is an individual or a company that provides Selegiline Hydrochloride active pharmaceutical ingredient (API) or Selegiline Hydrochloride finished formulations upon request. The Selegiline Hydrochloride suppliers may include Selegiline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Selegiline Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selegiline Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Selegiline Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Selegiline Hydrochloride DMFs exist exist since differing nations have different regulations, such as Selegiline Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Selegiline Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Selegiline Hydrochloride USDMF includes data on Selegiline Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Selegiline Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Selegiline Hydrochloride suppliers with USDMF on PharmaCompass.
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