TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI Technology & API Services
02 1Curia
03 1DMFs Not Supported
04 1Henan Lihua Pharmaceutical
05 1SIMS Srl
06 1Taisho Pharmaceutical
07 1Taro Pharmaceutical Industries
01 1HYDROCORTISONE 17-BUTYRATE USP, MICRONIZED
02 1HYDROCORTISONE BUTEPRATE
03 1HYDROCORTISONE BUTYRATE DRUG SUBSTANCE
04 1HYDROCORTISONE BUTYRATE USP
05 1HYDROCORTISONE BUTYRATE, MICRONIZED
06 2HYDROCORTISONE-17-BUTYRATE
01 1China
02 1Israel
03 1Italy
04 1Japan
05 2U.S.A
06 1Blank
01 4Active
02 3Inactive
01 2Complete
02 5Blank
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 : Complete
Rev. Date : 2013-01-09
Pay. Date : 2012-12-17
DMF Number : 21841
Submission : 2008-07-31
Status : Active
Type : II
USDMF
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
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31544
Submission : 2017-03-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4031
Submission : 1980-12-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8371
Submission : 1989-12-25
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-01-24
Pay. Date : 2015-03-06
DMF Number : 15750
Submission : 2001-12-06
Status : Active
Type : II
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.
A Hydrocortisone Butyrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Hydrocortisone Butyrate active pharmaceutical ingredient (API) in detail. Different forms of Hydrocortisone Butyrate DMFs exist exist since differing nations have different regulations, such as Hydrocortisone Butyrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Hydrocortisone Butyrate DMF submitted to regulatory agencies in the US is known as a USDMF. Hydrocortisone Butyrate USDMF includes data on Hydrocortisone Butyrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Hydrocortisone Butyrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Hydrocortisone Butyrate suppliers with USDMF on PharmaCompass.
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