EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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01 2EUROAPI
02 1LGM Pharma
03 1FARMAK, a.s
04 1Jai Radhe Sales
05 1TAPI Technology & API Services
06 1Anhui Biochem Pharmaceutical
07 2Anvitha Lifecare
08 1Apicore
09 1Catalent Pharma Solutions
10 2Catalytica
11 2Dipharma
12 1Embio Limited
13 1Heer Pharma
14 1Letco Medical
15 1Medisca
16 1Oceanic Pharmachem
17 1Pcca
18 1RICONPHARMA LLC
19 1Resolution Chemicals Limited
20 3Siegfried AG
21 1Stason Pharmaceuticals, Inc.
22 1Tianish Laboratories
23 1Trifarma
24 1Viatris
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02 1Czech Republic
03 2France
04 10India
05 1Israel
06 3Italy
07 3Switzerland
08 7U.S.A
09 2United Kingdom
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01 6Active
02 10Inactive
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01 4Valid
02 1Withdrawn by Holder
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01 1219MF10340
02 1229MF10114
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01 1WC-0046
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01 120210819-209-J-950
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01 138779-2792
02 145542-1146
03 146438-0062
04 146438-0642
05 151927-0129
06 160646-106
07 162991-1135
08 163278-0102
09 182231-113
10 184206-0083
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5161
Submission : 1983-12-01
Status : Active
Type : II
Certificate Number : R1-CEP 1998-014 - Rev 04
Issue Date : 2021-12-14
Type : Chemical
Substance Number : 1260
Status : Valid
Registration Number : 229MF10114
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2017-06-30
Latest Date of Registration :
NDC Package Code : 45542-1146
Start Marketing Date : 1989-06-06
End Marketing Date : 2026-01-19
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : CN |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Farmak works in the development, production and marketing of APIs, Intermediates & Specialties// FDA inspected.
NDC Package Code : 63278-0102
Start Marketing Date : 1997-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10235
Submission : 1993-05-05
Status : Inactive
Type : II
NDC Package Code : 82231-113
Start Marketing Date : 1989-06-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : CN |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9230
Submission : 1991-07-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11115
Submission : 1994-09-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10340
Submission : 1993-06-28
Status : Inactive
Type : II
Certificate Number : R1-CEP 1999-124 - Rev 04
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 1260
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9734
Submission : 1992-06-23
Status : Inactive
Type : II
47
PharmaCompass offers a list of Selegiline Hydrochloride 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 Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Selegiline Hydrochloride API Price utilized in the formulation of products. Selegiline Hydrochloride API Price is not always fixed or binding as the Selegiline Hydrochloride Price is obtained through a variety of data sources. The Selegiline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zelapar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zelapar, including repackagers and relabelers. The FDA regulates Zelapar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zelapar 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 Zelapar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zelapar supplier is an individual or a company that provides Zelapar active pharmaceutical ingredient (API) or Zelapar finished formulations upon request. The Zelapar suppliers may include Zelapar API manufacturers, exporters, distributors and traders.
click here to find a list of Zelapar suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 24 companies offering Zelapar
Get in contact with the supplier of your choice: