Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2Sanofi
02 1ACS DOBFAR SPA
03 1Fujifilm Diosynth Biotechnologies
04 1Pfizer Inc
05 1Pierrel
06 1SIMS Srl
07 1Blank
01 4TRIAMCINOLONE
02 1TRIAMCINOLONE ALCOHOL
03 1TRIAMCINOLONE AND RELATED PRODUCTS
04 1TRIAMCINOLONE MICRO
05 1TRIAMCINOLONE USP
01 2France
02 3Italy
03 1U.S.A
04 1United Kingdom
05 1Blank
01 8Inactive
01 8Blank
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 : 4081
Submission : 1981-03-03
Status : Inactive
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 : 6281
Submission : 1986-03-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2206
Submission : 1973-12-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3759
Submission : 1980-04-07
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2035
Submission : 1972-12-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2656
Submission : 1976-04-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6105
Submission : 1985-10-28
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5353
Submission : 1984-04-30
Status : Inactive
Type : II
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A Triamcinolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triamcinolone, including repackagers and relabelers. The FDA regulates Triamcinolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triamcinolone 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 Triamcinolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triamcinolone supplier is an individual or a company that provides Triamcinolone active pharmaceutical ingredient (API) or Triamcinolone finished formulations upon request. The Triamcinolone suppliers may include Triamcinolone API manufacturers, exporters, distributors and traders.
click here to find a list of Triamcinolone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Triamcinolone DMF (Drug Master File) is a document detailing the whole manufacturing process of Triamcinolone active pharmaceutical ingredient (API) in detail. Different forms of Triamcinolone DMFs exist exist since differing nations have different regulations, such as Triamcinolone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Triamcinolone DMF submitted to regulatory agencies in the US is known as a USDMF. Triamcinolone USDMF includes data on Triamcinolone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Triamcinolone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Triamcinolone suppliers with USDMF on PharmaCompass.
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