Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
01 1Pfizer CentreOne
02 1Symbiotec Pharmalab
03 1TAPI Technology & API Services
04 1Curia
05 1DMFs Not Supported
06 1Guangzhou Topwork Chemical
07 1Henan Lihua Pharmaceutical
08 1NEWCHEM SPA
09 1SIMS Srl
10 1Steroid SpA
11 1Symbiotica Specialty Ingredients
12 1Taisho Pharmaceutical
13 1Taro Pharmaceutical Industries
14 1Tianjin Pacific Chemical & Pharmaceutical Co., Ltd
15 1Zhejiang Xianju Pharmaceutical Co. Ltd
01 4China
02 1India
03 1Israel
04 3Italy
05 1Japan
06 1Malaysia
07 3U.S.A
08 1Blank
01 4Active
02 3Inactive
03 8Blank
01 15Blank
01 1222MF10261
02 1222MF10284
03 1223MF10022
04 12Blank
01 15Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18142
Submission : 2005-03-04
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31544
Submission : 2017-03-23
Status : Active
Type : II
NDC Package Code : 64958-0030
Start Marketing Date : 2006-08-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-01-24
Pay. Date : 2015-03-06
DMF Number : 15750
Submission : 2001-12-06
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8371
Submission : 1989-12-25
Status : Active
Type : II
NDC Package Code : 48246-100
Start Marketing Date : 1996-08-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (2kg/2kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-09
Pay. Date : 2012-12-17
DMF Number : 21841
Submission : 2008-07-31
Status : Active
Type : II
Registration Number : 222MF10284
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2010-12-27
Latest Date of Registration : --
NDC Package Code : 65089-0035
Start Marketing Date : 1982-03-31
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 : 4031
Submission : 1980-12-19
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 : 8264
Submission : 1989-11-22
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Registration Number : 223MF10022
Registrant's Address : Via de Amicis 47, 20123 Milano, Italy
Initial Date of Registration : 2011-02-08
Latest Date of Registration : --
NDC Package Code : 24002-0017
Start Marketing Date : 2009-07-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Hydrocortisone Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Butyrate, including repackagers and relabelers. The FDA regulates Hydrocortisone Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Butyrate 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 Butyrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Butyrate supplier is an individual or a company that provides Hydrocortisone Butyrate active pharmaceutical ingredient (API) or Hydrocortisone Butyrate finished formulations upon request. The Hydrocortisone Butyrate suppliers may include Hydrocortisone Butyrate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Butyrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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