Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1Pfizer CentreOne
02 1Coral Drugs Private Limited
03 2Axplora
04 1LGM Pharma
05 1Symbiotec Pharmalab
06 1TAPI Technology & API Services
07 1ACS DOBFAR SPA
08 1ASG Biochem
09 1Amphastar Pharmaceuticals
10 1Arudavis Labs
11 1Balaji Corporation
12 1Bayer AG
13 1Curia
14 1GD Searle LLC
15 1Hangzhou Think Chemical Co.Ltd
16 1Hanways Chempharm
17 1Hubei Gedian Humanwell Pharmaceutical
18 1Merck & Co
19 1Mortar & Pestle
20 1Naari
21 1Pfizer Inc
22 1SIMS Srl
23 1Sterling Spa
24 1Taizhou Taifa Pharmaceuticals Co. Ltd.
25 2Teva Pharmaceutical Industries
26 1YANCHENG XINYI PHARM AND CHEM CO LTD
27 1Zhejiang Xianju Pharmaceutical Co. Ltd
28 1Zhejiang Xianju Yangguang Bioproducts
29 1Blank
01 7China
02 3Germany
03 7India
04 3Israel
05 3Italy
06 7U.S.A
07 1Blank
01 11Active
02 7Inactive
03 13Blank
01 1Expired
02 6Valid
03 24Blank
01 1222MF10098
02 30Blank
01 31Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4975
Submission : 1983-07-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12695
Submission : 1997-10-15
Status : Active
Type : II
Certificate Number : R1-CEP 2002-191 - Rev 03
Issue Date : 2023-07-03
Type : Chemical
Substance Number : 673
Status : Valid
Registration Number : 222MF10098
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2010-03-17
Latest Date of Registration : --
NDC Package Code : 46439-8712
Start Marketing Date : 1992-02-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Saehan Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-58-B-142-01
Manufacturer Name : Farmabios SpA
Manufacturer Address : Farmabios SpA via Pavia 1 27027 GROPELLO CAIROLI-Pavia ITALY
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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 : 12703
Submission : 1997-10-20
Status : Active
Type : II
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-01-29
Pay. Date : 2014-09-03
DMF Number : 26389
Submission : 2012-09-04
Status : Active
Type : II
NDC Package Code : 46439-8712
Start Marketing Date : 1992-02-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Registrant Name : Saehan Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-58-B-142-01
Manufacturer Name : Farmabios SpA
Manufacturer Address : Farmabios SpA via Pavia 1 27027 GROPELLO CAIROLI-Pavia ITALY
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 27995
Submission : 2014-02-24
Status : Active
Type : II
NDC Package Code : 51508-017
Start Marketing Date : 2024-04-11
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 : 27546
Submission : 2014-10-22
Status : Active
Type : II
Certificate Number : R0-CEP 2015-001 - Rev 00
Issue Date : 2017-09-12
Type : Chemical
Substance Number : 673
Status : Expired
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-03-03
Pay. Date : 2014-12-22
DMF Number : 28800
Submission : 2014-11-12
Status : Active
Type : II
NDC Package Code : 65089-0002
Start Marketing Date : 1984-07-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-02-14
Pay. Date : 2021-09-30
DMF Number : 32282
Submission : 2018-02-08
Status : Active
Type : II
NDC Package Code : 52221-118
Start Marketing Date : 2016-10-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34977
Submission : 2020-07-02
Status : Active
Type : II
Certificate Number : R0-CEP 2019-336 - Rev 00
Issue Date : 2021-11-26
Type : Chemical
Substance Number : 673
Status : Valid
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-12-09
Pay. Date : 2013-09-25
DMF Number : 19433
Submission : 2006-05-10
Status : Active
Type : II
NDC Package Code : 60722-1006
Start Marketing Date : 2017-01-17
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 : 5389
Submission : 1984-05-11
Status : Active
Type : II
Certificate Number : R1-CEP 1995-051 - Rev 07
Issue Date : 2017-03-01
Type : Chemical
Substance Number : 673
Status : Valid
NDC Package Code : 12866-1099
Start Marketing Date : 2017-05-12
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 : 759
Submission : 1964-01-06
Status : Inactive
Type : II
NDC Package Code : 0009-0067
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2012-12-06
Registration Number : 20121206-58-B-340-07
Manufacturer Name : Pharmacia & Upjohn Company LLC
Manufacturer Address : 7000 Portage Road, Kalamazoo, MI 49001
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3747
Submission : 1980-03-11
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6488
Submission : 1986-07-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1988
Submission : 1972-08-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21563
Submission : 2008-01-15
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2724
Submission : 1976-08-11
Status : Inactive
Type : II
Certificate Number : R1-CEP 2002-048 - Rev 01
Issue Date : 2012-10-26
Type : Chemical
Substance Number : 673
Status : Valid
NDC Package Code : 64918-1941
Start Marketing Date : 2024-01-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 1999-153 - Rev 04
Issue Date : 2021-11-23
Type : Chemical
Substance Number : 673
Status : Valid
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 : 6007
Submission : 1985-07-30
Status : Inactive
Type : II
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A CAS-71-58-9 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-71-58-9, including repackagers and relabelers. The FDA regulates CAS-71-58-9 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-71-58-9 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 CAS-71-58-9 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAS-71-58-9 supplier is an individual or a company that provides CAS-71-58-9 active pharmaceutical ingredient (API) or CAS-71-58-9 finished formulations upon request. The CAS-71-58-9 suppliers may include CAS-71-58-9 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-71-58-9 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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