Axplora- The partner of choice for complex APIs.
01 1Axplora
02 1Aarti Pharmalabs
03 1TAPI Technology & API Services
04 1ACS DOBFAR SPA
05 2Bristol Myers Squibb
06 1NEWCHEM SPA
07 1Blank
01 1DESFLUORO TRIAMCINOLONE ACETONIDE
02 3DESONIDE
03 1DESONIDE (PREDNACINOLONE 16,17 ACETONIDE
04 1DESONIDE DRUG SUBSTANCE
05 1DESONIDE MICRONIZED
06 1DESONIDE, BULK, NON-STERILE, NON-MICRONIZED & MICRONIZED
01 1Germany
02 1India
03 1Israel
04 2Italy
05 2U.S.A
06 1Blank
01 3Active
02 5Inactive
01 2Complete
02 6Blank
GDUFA
DMF Review : Complete
Rev. Date : 2014-09-05
Pay. Date : 2014-09-03
DMF Number : 19574
Submission : 2006-07-06
Status : Active
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22963
Submission : 2009-07-20
Status : Active
Type : II
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-17
Pay. Date : 2014-01-14
DMF Number : 4420
Submission : 1982-02-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3100
Submission : 1978-01-03
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4008
Submission : 1980-12-05
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 1244
Submission : 1968-10-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22749
Submission : 2009-04-21
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5476
Submission : 1984-07-05
Status : Inactive
Type : II
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A Desonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desonide, including repackagers and relabelers. The FDA regulates Desonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desonide 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 Desonide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desonide supplier is an individual or a company that provides Desonide active pharmaceutical ingredient (API) or Desonide finished formulations upon request. The Desonide suppliers may include Desonide API manufacturers, exporters, distributors and traders.
click here to find a list of Desonide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Desonide DMF (Drug Master File) is a document detailing the whole manufacturing process of Desonide active pharmaceutical ingredient (API) in detail. Different forms of Desonide DMFs exist exist since differing nations have different regulations, such as Desonide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Desonide DMF submitted to regulatory agencies in the US is known as a USDMF. Desonide USDMF includes data on Desonide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Desonide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Desonide suppliers with USDMF on PharmaCompass.
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