EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 3EUROAPI
02 1Pfizer CentreOne
03 4Symbiotec Pharmalab
04 1Axplora
05 1Sanofi
06 1Rochem International Inc
07 1Gonane Pharma
08 1Pharm-RX Chemical
09 1HRV Global Life Sciences
10 1Bioquim
11 1Bayer AG
12 1Biotechnica DWC
13 1Capot Chemicals Co Ltd
14 3Curia
15 2Fujifilm Diosynth Biotechnologies
16 1Guangzhou Topwork Chemical
17 3Henan Lihua Pharmaceutical
18 1Hikma Pharmaceuticals
19 1J&H CHEM
20 1Jiangsu Lianhuan Pharmaceutical
21 1Jin Dun Medical
22 1Mac-Chem Products (India) Pvt.Ltd
23 1Maharshi Pharma Chem
24 1NEWCHEM SPA
25 1Pfizer Inc
26 1Prachem Laboratories
27 1Qingdao Qingmei Biotech
28 1Reliable Biopharmaceutical Corporation
29 2Shandong Xinhua Pharmaceutical
30 1Shanghai New Hualian Pharmaceutical
31 1SimSon Pharma
32 1Tecoland Corporation
33 2Tianjin Jinjin Pharmaceutical Co Ltd
34 1Tianjin Pharmaceutical Holdings Ltd
35 1Tianjin Tianyao Pharmaceuticals Co., Ltd.
36 1Vaishali Pharma Ltd
37 2Yangzhou Pharmaceutical
38 1Zhejiang Pure Pharmaceutical
39 1Zhejiang Xianju Pharmaceutical Co. Ltd
01 1Algeria
02 20China
03 4France
04 2Germany
05 11India
06 1Italy
07 1Spain
08 9U.S.A
09 3United Kingdom
01 19Active
02 10Inactive
03 23Blank
01 12Valid
02 2Withdrawn by Holder
03 38Blank
01 1217MF10680
02 1218MF10377
03 1220MF10093
04 1222MF10138
05 1226MF10036
06 1228MF10090
07 46Blank
01 2WC-0161A2
02 2WC-0162A2
03 1WC-0485A3
04 47Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2789
Submission : 1976-11-11
Status : Active
Type : II
Certificate Number : CEP 2019-166 - Rev 03
Issue Date : 2024-11-25
Type : Chemical
Substance Number : 335
Status : Valid
Registration Number : 220MF10093
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2008-03-28
Latest Date of Registration : --
NDC Package Code : 82298-101
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-07-25
Registration Number : 20230725-209-J-1524
Manufacturer Name : EUROAPI France
Manufacturer Address : 4 Lieu Dit La Paterie, Vertolaye, 63480, France
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-26
Pay. Date : 2013-02-13
DMF Number : 1413
Submission : 1969-09-02
Status : Active
Type : II
Certificate Number : R1-CEP 2002-220 - Rev 02
Issue Date : 2023-03-23
Type : Chemical
Substance Number : 335
Status : Valid
Registration Number : 222MF10138
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2010-04-14
Latest Date of Registration : --
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-02-09
Pay. Date : 2015-06-09
DMF Number : 29221
Submission : 2015-03-30
Status : Active
Type : II
Certificate Number : CEP 2018-054 - Rev 02
Issue Date : 2024-04-15
Type : Chemical
Substance Number : 335
Status : Valid
Date of Issue : 2022-09-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm :
NDC Package Code : 22552-0037
Start Marketing Date : 2013-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37639
Submission : 2023-01-24
Status : Active
Type : II
Available Reg Filing : EU |
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7416
Submission : 1988-04-04
Status : Inactive
Type : II
NDC Package Code : 50396-7004
Start Marketing Date : 2011-02-07
End Marketing Date : 2026-07-26
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-08-04
Pay. Date : 2016-04-08
DMF Number : 30373
Submission : 2016-03-03
Status : Active
Type : II
Certificate Number : R1-CEP 2012-163 - Rev 01
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 335
Status : Valid
Registration Number : 228MF10090
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2016-04-15
Latest Date of Registration : --
NDC Package Code : 82298-101
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-07-25
Registration Number : 20230725-209-J-1524
Manufacturer Name : EUROAPI France
Manufacturer Address : 4 Lieu Dit La Paterie, Vertolaye, 63480, France
Available Reg Filing : ASMF |
Certificate Number : R1-CEP 1996-052 - Rev 07
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 335
Status : Withdrawn by Holder
Registration Number : 218MF10377
Registrant's Address : 15 rue Traversie(')re 75012 Paris France
Initial Date of Registration : 2006-03-20
Latest Date of Registration : --
NDC Package Code : 82298-101
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-07-25
Registration Number : 20230725-209-J-1524
Manufacturer Name : EUROAPI France
Manufacturer Address : 4 Lieu Dit La Paterie, Vertolaye, 63480, France
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-12-27
Pay. Date : 2019-12-03
DMF Number : 31349
Submission : 2017-01-12
Status : Active
Type : II
Date of Issue : 2022-07-05
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm :
NDC Package Code : 22552-0037
Start Marketing Date : 2013-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Date of Issue : 2022-07-05
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm :
NDC Package Code : 22552-0037
Start Marketing Date : 2013-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm :
NDC Package Code : 22552-0037
Start Marketing Date : 2013-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28500
Submission : 2014-07-22
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-01-11
Pay. Date : 2021-09-15
DMF Number : 36074
Submission : 2021-08-05
Status : Active
Type : II
NDC Package Code : 81918-001
Start Marketing Date : 2023-03-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-08-24
Pay. Date : 2022-07-20
DMF Number : 35222
Submission : 2020-11-26
Status : Active
Type : II
NDC Package Code : 57582-013
Start Marketing Date : 2021-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-07-02
Pay. Date : 2014-12-16
DMF Number : 19734
Submission : 2006-09-06
Status : Active
Type : II
Certificate Number : R0-CEP 2021-048 - Rev 01
Issue Date : 2022-05-05
Type : Chemical
Substance Number : 335
Status : Valid
NDC Package Code : 61907-011
Start Marketing Date : 2019-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2021-07-05
Registration Number : 20210705-209-J-740
Manufacturer Name : Tianjin Jinjin Pharmaceutical Co., Ltd@Tianjin jinjin Pharmaceutical Co.,Ltd
Manufacturer Address : Industrial Zone of Zhangjiawo Town, Xiqing District Tianjin, China@Industrial Zone of Zhangjiawo Town, Xiqing District, Economic and Development Tianjin China
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-03-11
Pay. Date : 2020-11-09
DMF Number : 32204
Submission : 2017-10-22
Status : Active
Type : II
Certificate Number : R1-CEP 2015-033 - Rev 00
Issue Date : 2021-11-25
Type : Chemical
Substance Number : 335
Status : Valid
NDC Package Code : 61907-011
Start Marketing Date : 2019-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2021-07-05
Registration Number : 20210705-209-J-740
Manufacturer Name : Tianjin Jinjin Pharmaceutical Co., Ltd@Tianjin jinjin Pharmaceutical Co.,Ltd
Manufacturer Address : Industrial Zone of Zhangjiawo Town, Xiqing District Tianjin, China@Industrial Zone of Zhangjiawo Town, Xiqing District, Economic and Development Tianjin China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16089
Submission : 2002-08-06
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-07-15
Pay. Date : 2019-10-15
DMF Number : 33073
Submission : 2018-10-04
Status : Active
Type : II
NDC Package Code : 58624-0700
Start Marketing Date : 1984-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2020-12-17
Registration Number : 20201217-209-J-539
Manufacturer Name : Shandong Xinhua Pharmaceutical Co.,Ltd
Manufacturer Address : Hutian Chemical Industrial Zone, Zibo, Shandong, PR China
GDUFA
DMF Review : Reviewed
Rev. Date : 2023-12-12
Pay. Date : 2023-06-13
DMF Number : 30230
Submission : 2016-01-21
Status : Active
Type : II
Certificate Number : CEP 2018-239 - Rev 02
Issue Date : 2024-09-25
Type : Chemical
Substance Number : 335
Status : Valid
NDC Package Code : 60722-1001
Start Marketing Date : 2016-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2018-02-05
Registration Number : 20180205-209-J-16
Manufacturer Name : Zhejiang Xianju Pharmaceutical Co., Ltd.
Manufacturer Address : No.3 Donghai 4th Avenue, Zhejiang Toumen Port Economic Development Zone, Linhai, Zhejiang, China
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-10-07
Pay. Date : 2015-12-24
DMF Number : 28066
Submission : 2014-02-28
Status : Active
Type : II
NDC Package Code : 64958-0036
Start Marketing Date : 2003-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hiple Co., Ltd.
Registration Date : 2022-02-24
Registration Number : 20210711-209-J-980(4)
Manufacturer Name : Henan Lihua Pharmaceutical Co.,Ltd.
Manufacturer Address : Middle of Huanghe Street, Anyang Hi-Tech Industry Development Zone, China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7046
Submission : 1987-07-07
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 : 3917
Submission : 1980-07-17
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 : 4026
Submission : 1981-01-08
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11606
Submission : 1995-07-27
Status : Inactive
Type : II
Certificate Number : R0-CEP 2019-176 - Rev 00
Issue Date : 2021-10-06
Type : Chemical
Substance Number : 335
Status : Valid
NDC Package Code : 58624-0700
Start Marketing Date : 1984-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2020-12-17
Registration Number : 20201217-209-J-539
Manufacturer Name : Shandong Xinhua Pharmaceutical Co.,Ltd
Manufacturer Address : Hutian Chemical Industrial Zone, Zibo, Shandong, PR China
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8269
Submission : 1989-10-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18944
Submission : 2005-11-09
Status : Inactive
Type : II
Certificate Number : R0-CEP 2022-264 - Rev 00
Issue Date : 2023-08-22
Type : Chemical
Substance Number : 335
Status : Valid
Registration Number : 226MF10036
Registrant's Address : Middle of Huanghe Street, Anyang Hi-Tech Industry Development Zone, Henan, China
Initial Date of Registration : 2014-02-05
Latest Date of Registration : --
NDC Package Code : 64958-0036
Start Marketing Date : 2003-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hiple Co., Ltd.
Registration Date : 2022-02-24
Registration Number : 20210711-209-J-980(4)
Manufacturer Name : Henan Lihua Pharmaceutical Co.,Ltd.
Manufacturer Address : Middle of Huanghe Street, Anyang Hi-Tech Industry Development Zone, China
A Hydrocortisone Sodium Phosphate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Sodium Phosphate, including repackagers and relabelers. The FDA regulates Hydrocortisone Sodium Phosphate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Sodium Phosphate 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 Hydrocortisone Sodium Phosphate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Sodium Phosphate supplier is an individual or a company that provides Hydrocortisone Sodium Phosphate active pharmaceutical ingredient (API) or Hydrocortisone Sodium Phosphate finished formulations upon request. The Hydrocortisone Sodium Phosphate suppliers may include Hydrocortisone Sodium Phosphate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Sodium Phosphate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 39 companies offering Hydrocortisone Sodium Phosphate
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