EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI
02 1Pfizer CentreOne
03 1Symbiotec Pharmalab
04 1Transo-Pharm USA LLC
05 2Gonane Pharma
06 1HRV Global Life Sciences
07 1Bioquim
08 1ACS DOBFAR SPA
09 1Arihantanam Life Care
10 1Bayer AG
11 1Biofer
12 1Curia
13 1DMFs Not Supported
14 2Fujifilm Diosynth Biotechnologies
15 1Jiangsu Lianhuan Pharmaceutical
16 1Mac-Chem Products (India) Pvt.Ltd
17 1Mutual Corporation
18 1NEWCHEM SPA
19 2Pfizer Inc
20 1Quimica Sintetica
21 1SIMS Srl
22 1Symbiotica Specialty Ingredients
01 1China
02 1France
03 1Germany
04 6India
05 4Italy
06 1Japan
07 1Malaysia
08 2Spain
09 5U.S.A
10 2United Kingdom
11 1Blank
01 7Inactive
02 18Blank
01 6Valid
02 1Withdrawn by Holder
03 18Blank
01 1219MF10308
02 24Blank
01 1WC-0162A2
02 1WC-0275
03 23Blank
Certificate Number : R0-CEP 2020-246 - Rev 01
Issue Date : 2021-12-16
Type : Chemical
Substance Number : 768
Status : Valid
Certificate Number : R1-CEP 2014-120 - Rev 01
Issue Date : 2021-08-19
Type : Chemical
Substance Number : 768
Status : Valid
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162A2
Address of the Firm :
NDC Package Code : 22552-0007
Start Marketing Date : 2017-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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.
Gonane has API manufacturing expertise in new-age Corticosteroids, Hormones and other pharma raw materials.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2889
Submission : 1977-03-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6753
Submission : 1986-11-26
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 : 3961
Submission : 1980-10-06
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 : 4122
Submission : 1981-04-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6185
Submission : 1986-01-30
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 : 6646
Submission : 1986-10-27
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3097
Submission : 1978-01-09
Status : Inactive
Type : II
Registration Number : 219MF10308
Registrant's Address : 2-6-2 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2007-10-05
Latest Date of Registration : --
Certificate Number : R0-CEP 2019-039 - Rev 02
Issue Date : 2023-04-21
Type : Chemical
Substance Number : 768
Status : Valid
Certificate Number : R0-CEP 2000-390 - Rev 00
Issue Date : 2001-12-07
Type : TSE
Substance Number : 768
Status : Withdrawn by Holder
Certificate Number : CEP 2005-187 - Rev 03
Issue Date : 2024-08-29
Type : Chemical
Substance Number : 768
Status : Valid
Date of Issue : 2021-01-22
Valid Till : 2023-08-01
Written Confirmation Number : WC-0275
Address of the Firm :
Certificate Number : R1-CEP 2015-183 - Rev 00
Issue Date : 2021-10-07
Type : Chemical
Substance Number : 768
Status : Valid
Certificate Number : CEP 2023-257 - Rev 00
Issue Date : 2024-07-19
Type : Chemical
Substance Number : 768
Status : Valid
A Hydrocortisone Sodium Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Sodium Succinate, including repackagers and relabelers. The FDA regulates Hydrocortisone Sodium Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Sodium Succinate 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 Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Sodium Succinate supplier is an individual or a company that provides Hydrocortisone Sodium Succinate active pharmaceutical ingredient (API) or Hydrocortisone Sodium Succinate finished formulations upon request. The Hydrocortisone Sodium Succinate suppliers may include Hydrocortisone Sodium Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Sodium Succinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 21 companies offering Hydrocortisone Sodium Succinate
Get in contact with the supplier of your choice:
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