HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
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01 1HRV Global Life Sciences
02 1Octavius Pharma Pvt. Ltd
03 1Aspire Lifesciences Pvt Ltd
04 2Bayer AG
05 1Cambrex Corporation
06 1Corden Pharma Bergamo S.p.A
07 1Divis Laboratories
08 1Fine Organics
09 1Jiangsu Recbio Technology
10 1SALSBURY CHEMICALS INC
11 1Shanghai Ziyuan Pharmaceutical
12 1Solara Active Pharma Sciences
13 1Valens Molecules
14 2Virchow Group
15 1Zhejiang Hisoar Pharmaceutical
16 2Zhejiang Jiuzhou Pharmaceutical
17 2Blank
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01 5China
02 2Germany
03 8India
04 1Italy
05 2U.S.A
06 1United Kingdom
07 2Blank
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01 1Active
02 11Inactive
03 9Blank
01 3Valid
02 2Withdrawn by Holder
03 16Blank
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01 1219MF10098
02 1301MF10008
03 1306MF10016
04 18Blank
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01 1WC-0235A1
02 1WC-235
03 19Blank
Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16817
Submission : 2003-09-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14688
Submission : 2000-01-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8886
Submission : 1990-12-10
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17649
Submission : 2004-08-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22238
Submission : 2008-11-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14724
Submission : 2000-02-23
Status : Inactive
Type : II
Certificate Number : R1-CEP 2002-088 - Rev 02
Issue Date : 2015-03-20
Type : Chemical
Substance Number : 863
Status : Valid
Registration Number : 306MF10016
Registrant's Address : Waisha Road 99# Jiaojiang Taizhou City, Zhejiang China
Initial Date of Registration : 2024-01-24
Latest Date of Registration :
Registrant Name : Medica Korea Co., Ltd.
Registration Date : 2012-02-24
Registration Number : 20091224-105-F-46-02(1)
Manufacturer Name : Zhejiang Jizhou Pharmaceutical Co., Ltd.
Manufacturer Address : 99 waisha Road, Jiaojiang District, Taizhou City, Zhejiang province, 318000, China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 14751
Submission : 2000-03-08
Status : Inactive
Type : II
Registrant Name : Medica Korea Co., Ltd.
Registration Date : 2012-02-24
Registration Number : 20091224-105-F-46-02(1)
Manufacturer Name : Zhejiang Jizhou Pharmaceutical Co., Ltd.
Manufacturer Address : 99 waisha Road, Jiaojiang District, Taizhou City, Zhejiang province, 318000, China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11163
Submission : 1994-10-26
Status : Inactive
Type : II
Certificate Number : R1-CEP 2004-278 - Rev 02
Issue Date : 2017-12-20
Type : Chemical
Substance Number : 863
Status : Withdrawn by Holder
NDC Package Code : 49964-0018
Start Marketing Date : 2009-11-16
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 : 5145
Submission : 1983-10-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7242
Submission : 1987-11-09
Status : Inactive
Type : II
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 : 6489
Submission : 1986-07-17
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 : 7127
Submission : 1987-08-17
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Date of Issue : 2020-05-12
Valid Till : 2022-07-02
Written Confirmation Number : WC-0235A1
Address of the Firm :
Certificate Number : R1-CEP 2016-225 - Rev 00
Issue Date : 2022-01-10
Type : Chemical
Substance Number : 863
Status : Withdrawn by Holder
Date of Issue : 2019-11-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-235
Address of the Firm :
Certificate Number : R1-CEP 1996-040 - Rev 02
Issue Date : 2007-08-30
Type : Chemical
Substance Number : 863
Status : Valid
Registration Number : 219MF10098
Registrant's Address : 1205 11th Street, Charles City, Iowa, U.S. S. A.
Initial Date of Registration : 2007-03-14
Latest Date of Registration :
NDC Package Code : 59116-0630
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Goodwills Co., Ltd.
Registration Date : 2013-02-21
Registration Number : 20130221-105-F-60-04
Manufacturer Name : Cambrex Charles City, Inc.
Manufacturer Address : 1205 11th Street Charles City, Iowa 50616
Certificate Number : R1-CEP 2016-085 - Rev 00
Issue Date : 2023-01-19
Type : Chemical
Substance Number : 863
Status : Valid
Registration Number : 301MF10008
Registrant's Address : 202, SV'S Classic Residency, 6-3-853/2, Ameerpet, Hyderabad, Telangana-500 016, INDIA
Initial Date of Registration : 2019-05-28
Latest Date of Registration :
NDC Package Code : 62705-0222
Start Marketing Date : 2017-01-05
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 : 2017-01-17
Registration Number : 20150610-105-F-82-05(A)
Manufacturer Name : Valens Molecules Pvt. Ltd.
Manufacturer Address : Plot No. 11, Road No. 2, Industrial Estate, Medchal. Hyderabad-501 401, Telangana State, India
81
PharmaCompass offers a list of Sulfasalazine 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 Sulfasalazine manufacturer or Sulfasalazine supplier for your needs.
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A Sulfasalazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfasalazine, including repackagers and relabelers. The FDA regulates Sulfasalazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfasalazine 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 Sulfasalazine supplier is an individual or a company that provides Sulfasalazine active pharmaceutical ingredient (API) or Sulfasalazine finished formulations upon request. The Sulfasalazine suppliers may include Sulfasalazine API manufacturers, exporters, distributors and traders.
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We have 16 companies offering Sulfasalazine
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