Mysoline - 66490-691-10 - (Primidone)

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Drug Information of Mysoline

Product NDC: 66490-691
Proprietary Name: Mysoline
Non Proprietary Name: Primidone
Active Ingredient(s): 250    mg/1 & nbsp;   Primidone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Mysoline

Product NDC: 66490-691
Labeler Name: Valeant Pharmaceuticals North America
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009170
Marketing Category: NDA
Start Marketing Date: 20090624

Package Information of Mysoline

Package NDC: 66490-691-10
Package Description: 100 TABLET in 1 BOTTLE (66490-691-10)

NDC Information of Mysoline

NDC Code 66490-691-10
Proprietary Name Mysoline
Package Description 100 TABLET in 1 BOTTLE (66490-691-10)
Product NDC 66490-691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090624
Marketing Category Name NDA
Labeler Name Valeant Pharmaceuticals North America
Substance Name PRIMIDONE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Mysoline


General Information