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FOSPHENYTOIN

 
 
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

Drug Recalls
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…

Cerebyx (Fosphenytoin Sodium injection) Warner-Lambert NDA 20-450/S4, 20-450/S5 | Fosphenytoin Sodium Injection, Bedford Labs, Tentative Approval | Fosphenytoin Sodium Injection, Hospira, Tentative Approval | Fosphenytoin Sodium Injection, Abraxis Pharma, Tentative Approval | Fosphenytoin Sodium Injection, IV Therapeutics, Tentative Approval | Fosphenytoin Sodium Injection, Baxter Healthcare, Tentative Approval | Fosphenytoin Sodium Injection, Wockhardt Inc., Tentative Approval | Fosphenytoin Sodium Injection, Apotex Corp., Tentative Approval | Fosphenytoin Sodium Injection, Baxter Healthcare, Approval | Fosphenytoin Sodium Injection, PharmaForce Inc., Approval | Fosphenytoin Sodium Injection, Bedford Labs, Approval | Fosphenytoin Sodium Injection, Apotex, Approval | Fosphenytoin Sodium Injection, Hospira Inc., Approval | Fosphenytoin Sodium Injection, Wockhardt, Approval | Fosphenytoin Sodium Injection, Abraxis Pharma, Approval | Fosphenytoin Sodium Injection, Teva Parenteral, Approval | Fosphenytoin Sodium Injection, Akorn-Strides, LLC, Approval | Fosphenytoin Sodium Injection, Sun Pharmaceutical Industries, Inc., Approval

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


 

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