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SEVOFLURANE

 
 
Content specific to this active ingredient…

Drug Information
Prescribing and patient information from leading authorities

Drug Master Files
Type 2 master files on file at the FDA

Safety Information
For prescription drugs containing this active ingredient

Exclusivity
Patent and market exclusivity data

Federal Register
FR search results for this API

FDA Approved Labelling
Information found in this drug's package inserts

Research Links
Chemical identification and research citations

Title 21 Code of Federal Regulations
FDA regulations for this API

 
 
 
 
 
 
 
 

 


 

FDA Approval Activities for this Drug…

Sevoflurane Inhalation, 100%, Baxter Healthcare ANDA 75-895 Ultane (sevoflurane) Volatile Liquid for Inhalation, Abbott NDA 20-478/S-012 6/27/03 7/6/03 Ultane (sevoflurane), Abbott NDA 20-478/S-007 12/11/02 1/29/03 Ultane (sevoflurane), Abbott NDA 20-478/S-006 SEVOFLURANE Liquid; Inhalation 100% ULTANE Abbott 075895 AN SEVOFLURANE Liquid; Inhalation 100% SEVOFLURANE Baxter | Ultane (sevoflurane), Abbott Laboratories, Labeling Revision | Ultane (sevoflurane), Abbott Labs, Labeling Revision | Sojourn (Sevoflurane) Inhalation Liquid, Minrad Inc., Approval | Sevoflurane Liquid Inhalation, Halocarbon Products, Tentative Approval | Sevoflurane Liquid Inhalation, Halocarbon Products, Approval | Ultane (sevoflurane) Liquid Inhalation, Abbott Laboratories, Labeling Revision

^ FDA's latest approval appears at the bottom of this list. ^

                                                                   

 

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