Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
Reset all filters
01 1Bioquim
02 1Pfizer CentreOne
03 1Symbiotec Pharmalab
04 1TAPI Technology & API Services
05 1Alfa Chemistry
06 1Curia
07 1Guangzhou Topwork Chemical
08 1Henan Lihua Pharmaceutical
09 1NEWCHEM SPA
10 1SIMS Srl
11 1Steroid SpA
12 1Symbiotica
13 1Taisho Pharmaceutical
14 1Taro Pharmaceutical Industries
15 1Tianjin Pacific Chemical & Pharmaceutical Co., Ltd
16 1Tianjin Tianfa Pharmaceutical Import & Export
17 1Zhejiang Xianju Pharmaceutical Co. Ltd
Reset all filters
01 5China
02 1India
03 1Israel
04 3Italy
05 1Japan
06 1Malaysia
07 1Spain
08 4U.S.A
Reset all filters
01 4Active
02 2Inactive
03 11Blank
01 17Blank
Reset all filters
01 1222MF10261
02 1222MF10284
03 1223MF10022
04 14Blank
Reset all filters
01 17Blank
Reset all filters
01 17Blank
Reset all filters
01 124002-0017
02 148246-100
03 152128-130
04 164958-0030
05 165089-0035
06 12Blank
01 17Blank
Bioquim: An European GMP-certified company manufacturing bulk APIs, specializing in sterile lyophilization and chemical synthesis.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18142
Submission : 2005-03-04
Status : Inactive
Type : II
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 : 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 : 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
Product Not Available For Sales
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 : 4031
Submission : 1980-12-19
Status : Inactive
Type : II
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 : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
68
PharmaCompass offers a list of Hydrocortisone Butyrate 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 Hydrocortisone Butyrate manufacturer or Hydrocortisone Butyrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Butyrate manufacturer or Hydrocortisone Butyrate supplier.
PharmaCompass also assists you with knowing the Hydrocortisone Butyrate API Price utilized in the formulation of products. Hydrocortisone Butyrate API Price is not always fixed or binding as the Hydrocortisone Butyrate Price is obtained through a variety of data sources. The Hydrocortisone Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bucort manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bucort, including repackagers and relabelers. The FDA regulates Bucort manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bucort 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 Bucort manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bucort supplier is an individual or a company that provides Bucort active pharmaceutical ingredient (API) or Bucort finished formulations upon request. The Bucort suppliers may include Bucort API manufacturers, exporters, distributors and traders.
click here to find a list of Bucort suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 17 companies offering Bucort
Get in contact with the supplier of your choice: