LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 1LGM Pharma
02 1Seqens
03 2Chemische Fabrik Berg
04 1Excella GmbH
05 1Jai Radhe Sales
06 1Moehs Iberica
07 1TAPI Technology & API Services
08 1AASraw Biochemical Technology Co., Ltd
09 1ASG Biochem
10 1Arevipharma
11 1Asia Pioneer Pharmaceuticals
12 1Aspire Lifesciences Pvt Ltd
13 1Astellas Pharma
14 1Asymchem Laboratories
15 1Aurobindo Pharma Limited
16 1Bo-Chem Pvt Ltd
17 1Fareva
18 1Nishchem International Pvt. Ltd
19 2Olon S.p.A
20 1Remedy Labs
21 1SLN Pharmachem
22 1Sakar Healthcare
23 2Shouyuan Chemical
24 1Teva Pharmaceutical Industries
25 2Yangtze River Pharmaceutical Group
26 4Blank
01 6China
02 1France
03 4Germany
04 9India
05 2Israel
06 2Italy
07 1Japan
08 1Luxembourg
09 1Spain
10 2U.S.A
11 4Blank
01 4Active
02 7Inactive
03 22Blank
01 5Valid
02 1Withdrawn by Holder
03 27Blank
01 1218MF10150
02 1219MF10242
03 1306MF10097
04 1306MF10120
05 29Blank
01 33Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10150
Registrant's Address : 21, chemin de la Sauvegarde 21 Ecully Parc - CS 33167 69134 Ecully Cedex France
Initial Date of Registration : 2006-01-31
Latest Date of Registration : --
Available Reg Filing : CA |
Certificate Number : CEP 2022-463 - Rev 01
Issue Date : 2024-09-27
Type : Chemical
Substance Number : 1046
Status : Valid
NDC Package Code : 65319-1051
Start Marketing Date : 2020-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-08-05
Registration Number : 20200623-209-J-492(2)
Manufacturer Name : Chemische Fabrik Berg GmbH@Benechim SPRL
Manufacturer Address : Mainthalstraβe 3, 06749 Bitterfeld-Wolfen, Germany@Rue Rene Magritte 163 Lessines 7860 Belgium
Registration Number : 306MF10097
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2024-07-11
Latest Date of Registration : --
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 : 2014-10-01
Pay. Date : 2013-10-24
DMF Number : 5500
Submission : 1984-08-15
Status : Active
Type : II
Certificate Number : R1-CEP 2002-242 - Rev 05
Issue Date : 2022-06-13
Type : Chemical
Substance Number : 1046
Status : Valid
NDC Package Code : 65319-1051
Start Marketing Date : 2020-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-08-05
Registration Number : 20200623-209-J-492(2)
Manufacturer Name : Chemische Fabrik Berg GmbH@Benechim SPRL
Manufacturer Address : Mainthalstraβe 3, 06749 Bitterfeld-Wolfen, Germany@Rue Rene Magritte 163 Lessines 7860 Belgium
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-10-04
Pay. Date : 2013-09-26
DMF Number : 5204
Submission : 1983-12-22
Status : Active
Type : II
Certificate Number : R1-CEP 1996-098 - Rev 09
Issue Date : 2020-03-11
Type : Chemical
Substance Number : 1046
Status : Valid
Registration Number : 219MF10242
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2007-07-17
Latest Date of Registration : --
NDC Package Code : 46014-1015
Start Marketing Date : 2000-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-06-14
Registration Number : 20210614-209-J-893
Manufacturer Name : Excella GmbH & Co. KG
Manufacturer Address : Nürnberger Str. 12, 90537 Feucht, Germany
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34297
Submission : 2019-11-18
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-09-12
Pay. Date : 2018-09-04
DMF Number : 6735
Submission : 1986-12-15
Status : Active
Type : II
Certificate Number : R2-CEP 1995-016 - Rev 05
Issue Date : 2020-08-20
Type : Chemical
Substance Number : 1046
Status : Valid
NDC Package Code : 17337-0034
Start Marketing Date : 2012-12-05
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 : 27466
Submission : 2013-08-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19284
Submission : 2006-03-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5060
Submission : 1983-06-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21757
Submission : 2008-06-05
Status : Inactive
Type : II
NDC Package Code : 17337-0034
Start Marketing Date : 2012-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4734
Submission : 1982-12-01
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4793
Submission : 1983-01-12
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9531
Submission : 1992-01-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : R1-CEP 2005-197 - Rev 01
Issue Date : 2013-05-17
Type : Chemical
Substance Number : 1046
Status : Withdrawn by Holder
A Tamoxifen Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tamoxifen Citrate, including repackagers and relabelers. The FDA regulates Tamoxifen Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tamoxifen Citrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tamoxifen Citrate supplier is an individual or a company that provides Tamoxifen Citrate active pharmaceutical ingredient (API) or Tamoxifen Citrate finished formulations upon request. The Tamoxifen Citrate suppliers may include Tamoxifen Citrate API manufacturers, exporters, distributors and traders.
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