Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 1Sanofi
02 1Zhejiang Hengkang Pharmaceutical
03 1TAPI Technology & API Services
04 1Aarti Drugs
05 1Biotechnica DWC
06 1Curia
07 1DEAFARMA
08 1Erregierre SpA
09 1F. Hoffmann-La Roche
10 1HELM Portugal
11 1Liaoyuan Pharmaceutical
12 1ORGAMOL PHARMA SOLUTIONS SA
13 1RPG Life Sciences
14 1SIMS Srl
15 1Sato Yakuhin Kogyo Co., Ltd
16 1Shilpa Medicare
17 1Sicor Societa Italiana Corticosteroidi Srl
18 1Siegfried AG
19 1Teva Pharmaceutical Industries
20 1Zhejiang Sanmen Kangning Chemical
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01 1Algeria
02 3China
03 1France
04 3India
05 2Israel
06 4Italy
07 1Japan
08 1Portugal
09 3Switzerland
10 1U.S.A
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01 4Active
02 3Inactive
03 13Blank
01 6Valid
02 2Withdrawn by Holder
03 12Blank
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01 1219MF10156
02 1219MF10159
03 1219MF10251
04 1219MF10303
05 1222MF10127
06 1223MF10137
07 14Blank
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01 1WC-0253
02 19Blank
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01 120211209-209-J-1175
02 19Blank
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01 112660-0501
02 148292-0033
03 149706-0331
04 155486-1565
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01 20Blank
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : CEP 2000-052 - Rev 03
Issue Date : 2024-02-07
Type : Chemical
Substance Number : 1050
Status : Valid
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Registration Number : 223MF10137
Registrant's Address : No. 1 Longxiang Road, Hairun Street, Sanmen, Zhejiang, China
Initial Date of Registration : 2011-08-19
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 : N/A
Rev. Date :
Pay. Date :
DMF Number : 11664
Submission : 1995-09-21
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10492
Submission : 1993-09-15
Status : Active
Type : II
Certificate Number : R1-CEP 2002-106 - Rev 02
Issue Date : 2015-02-09
Type : Chemical
Substance Number : 1050
Status : Valid
NDC Package Code : 12660-0501
Start Marketing Date : 1979-02-01
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 : 11968
Submission : 1996-05-17
Status : Active
Type : II
Certificate Number : R1-CEP 1999-081 - Rev 02
Issue Date : 2017-07-17
Type : Chemical
Substance Number : 1050
Status : Valid
NDC Package Code : 49706-0331
Start Marketing Date : 2010-01-08
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 : 12643
Submission : 1997-09-04
Status : Active
Type : II
NDC Package Code : 55486-1565
Start Marketing Date : 2012-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22355
Submission : 2008-12-30
Status : Inactive
Type : II
Certificate Number : CEP 2002-116 - Rev 03
Issue Date : 2023-10-11
Type : Chemical
Substance Number : 1050
Status : Valid
Date of Issue : 2022-08-08
Valid Till : 2025-08-09
Written Confirmation Number : WC-0253
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3599
Submission : 1979-08-22
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8092
Submission : 1989-06-01
Status : Inactive
Type : II
Certificate Number : R1-CEP 2004-109 - Rev 03
Issue Date : 2021-05-03
Type : Chemical
Substance Number : 1050
Status : Valid
Registration Number : 219MF10251
Registrant's Address : Zhejiang Provincial Chemical and Medical Raw Material Base Linhai Zone Duqiao town, Linhai City, Zhejiang Province, China
Initial Date of Registration : 2007-07-26
Latest Date of Registration :
Registrant Name : Goodwills Co., Ltd.
Registration Date : 2021-12-09
Registration Number : 20211209-209-J-1175
Manufacturer Name : Zhejiang Liaoyuan Pharmaceutical Co., Ltd.
Manufacturer Address : Zhejiang Provincial Chemical and Medical Raw Materials Base Linhai Zone, Duqiao Town, Linhai City, Zhejiang Province, 317016, China
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PharmaCompass offers a list of Ticlopidine 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 Ticlopidine manufacturer or Ticlopidine supplier for your needs.
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A Tiklid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiklid, including repackagers and relabelers. The FDA regulates Tiklid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiklid 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 Tiklid supplier is an individual or a company that provides Tiklid active pharmaceutical ingredient (API) or Tiklid finished formulations upon request. The Tiklid suppliers may include Tiklid API manufacturers, exporters, distributors and traders.
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