Capital Farma, a leading European pharmaceutical company focusing on the development & distribution of niche APIs & Pharma Services.
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01 1Capital Farma
02 1Metrochem API Private Limited
03 1HRV Global Life Sciences
04 1TAPI Technology & API Services
05 2Ajinomoto Company
06 2Aurobindo Pharma Limited
07 1Credo Life Sciences
08 1Indena
09 2Johnson & Johnson Innovative Medicine
10 1Jubilant Generics
11 1Jubilant Pharmova
12 1Nanjing Bold Chemical
13 1Nortec Quimica
14 1Pellets Pharma Limited
15 1Polaris AI Pharma
16 1Ravoos Laboratories
17 2Sanochemia Pharmazeutika GmbH
18 3ScinoPharm Taiwan Ltd
19 1Sun Pharmaceutical Industries Limited
20 1Teva Pharmaceutical Industries
21 1Wuhan Shiji Pharmaceutical
22 1ZHEJIANG YIXIN PHARMACEUTICAL CO LTD
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01 2Austria
02 1Brazil
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08 1South Korea
09 1Spain
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11 2U.S.A
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01 7Active
02 8Inactive
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01 7Valid
02 1Withdrawn by Holder
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01 1230MF10065
02 1231MF10027
03 1231MF10054
04 1306MF10088
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01 1WC-0023
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01 120210510-209-J-776
02 120210610-209-J-538
03 120211012-209-J-1119
04 120211015-209-J-1014
05 120211015-209-J-1014(1)
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01 112578-890
02 147848-023
03 155111-081
04 165129-1113
05 165129-1332
06 165372-1138
07 165862-487
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Capital Farma, a leading European pharmaceutical company focusing on the development & distribution of niche APIs & Pharma Services.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-12-05
Pay. Date : 2012-11-08
DMF Number : 18112
Submission : 2005-02-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26643
Submission : 2012-11-26
Status : Active
Type : II
Certificate Number : CEP 2023-389 - Rev 00
Issue Date : 2024-06-19
Type : Chemical
Substance Number : 2366
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17972
Submission : 2005-01-05
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-08-24
Pay. Date : 2015-08-17
DMF Number : 17863
Submission : 2004-12-01
Status : Active
Type : II
Certificate Number : CEP 2011-011 - Rev 02
Issue Date : 2024-10-21
Type : Chemical
Substance Number : 2366
Status : Valid
Registration Number : 230MF10065
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
Initial Date of Registration : 2018-05-15
Latest Date of Registration :
NDC Package Code : 65129-1332
Start Marketing Date : 2013-09-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hyundai Pharmaceutical Co., Ltd.
Registration Date : 2021-10-12
Registration Number : 20211012-209-J-1119
Manufacturer Name : ScinoPharm Taiwan, Ltd.
Manufacturer Address : No. 1, Nan-ke 8th Road, Shan-Hua, Tainan 741014, Taiwan
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27564
Submission : 2013-12-30
Status : Active
Type : II
NDC Package Code : 65129-1113
Start Marketing Date : 2004-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17967
Submission : 2005-01-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18114
Submission : 2005-02-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Galantamine Hydrobromide 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 Galantamine Hydrobromide manufacturer or Galantamine Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Galantamine Hydrobromide API Price utilized in the formulation of products. Galantamine Hydrobromide API Price is not always fixed or binding as the Galantamine Hydrobromide Price is obtained through a variety of data sources. The Galantamine Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nivalin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nivalin, including repackagers and relabelers. The FDA regulates Nivalin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nivalin 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 Nivalin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nivalin supplier is an individual or a company that provides Nivalin active pharmaceutical ingredient (API) or Nivalin finished formulations upon request. The Nivalin suppliers may include Nivalin API manufacturers, exporters, distributors and traders.
click here to find a list of Nivalin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 22 companies offering Nivalin
Get in contact with the supplier of your choice: