EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI
02 1Pfizer CentreOne
03 2Symbiotec Pharmalab
04 1Axplora
05 1Sanofi
06 1Bayer AG
07 3Curia
08 2Fujifilm Diosynth Biotechnologies
09 3Henan Lihua Pharmaceutical
10 1Hikma Pharmaceuticals
11 1Jiangsu Lianhuan Pharmaceutical
12 1Reliable Biopharmaceutical Corporation
13 2Shandong Xinhua Pharmaceutical
14 1Shanghai New Hualian Pharmaceutical
15 2Tianjin Jinjin Pharmaceutical Co Ltd
16 1Tianjin Pharmaceutical Holdings Ltd
17 1Tianjin Tianyao Pharmaceuticals Co., Ltd.
18 2Yangzhou Pharmaceutical
19 1Zhejiang Xianju Pharmaceutical Co. Ltd
01 9HYDROCORTISONE
02 1HYDROCORTISONE BASE
03 1HYDROCORTISONE BASE & ACETATE
04 1HYDROCORTISONE BASE USP BULK API
05 1HYDROCORTISONE HEMISUCCINATE
06 1HYDROCORTISONE HEMISUCCINATE MICRONIZED AND NON-MICRONIZED
07 1HYDROCORTISONE HEMISUCCINATE USP
08 1HYDROCORTISONE M
09 2HYDROCORTISONE MICRONIZED
10 1HYDROCORTISONE MICRONIZED AND NON-MICRONIZED
11 3HYDROCORTISONE SODIUM PHOSPHATE
12 4HYDROCORTISONE USP
13 1HYDROCORTISONE, NON-STERILE, BULK DRUG SUBSTANCE
14 1HYDROCORTISONE, USP
15 1PHOSPHATE BUFFERED SALINE (PBS) POLYHESIVE HYDROCORTISONE SYRUP
01 14China
02 3France
03 2Germany
04 2India
05 5U.S.A
06 3United Kingdom
01 19Active
02 10Inactive
01 14Complete
02 15Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2789
Submission : 1976-11-11
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-26
Pay. Date : 2013-02-13
DMF Number : 1413
Submission : 1969-09-02
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-02-09
Pay. Date : 2015-06-09
DMF Number : 29221
Submission : 2015-03-30
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37639
Submission : 2023-01-24
Status : Active
Type : II
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
GDUFA
DMF Review : Complete
Rev. Date : 2016-08-04
Pay. Date : 2016-04-08
DMF Number : 30373
Submission : 2016-03-03
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-12-27
Pay. Date : 2019-12-03
DMF Number : 31349
Submission : 2017-01-12
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-10-07
Pay. Date : 2015-12-24
DMF Number : 28066
Submission : 2014-02-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16089
Submission : 2002-08-06
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-07-02
Pay. Date : 2014-12-16
DMF Number : 19734
Submission : 2006-09-06
Status : Active
Type : II
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.
A Hydrocortisone Sodium Phosphate DMF (Drug Master File) is a document detailing the whole manufacturing process of Hydrocortisone Sodium Phosphate active pharmaceutical ingredient (API) in detail. Different forms of Hydrocortisone Sodium Phosphate DMFs exist exist since differing nations have different regulations, such as Hydrocortisone Sodium Phosphate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hydrocortisone Sodium Phosphate DMF submitted to regulatory agencies in the US is known as a USDMF. Hydrocortisone Sodium Phosphate USDMF includes data on Hydrocortisone Sodium Phosphate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hydrocortisone Sodium Phosphate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hydrocortisone Sodium Phosphate suppliers with USDMF on PharmaCompass.
We have 19 companies offering Hydrocortisone Sodium Phosphate
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