Primidone - 50268-687-15 - (Primidone)

Alphabetical Index


Drug Information of Primidone

Product NDC: 50268-687
Proprietary Name: Primidone
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 Primidone

Product NDC: 50268-687
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040866
Marketing Category: ANDA
Start Marketing Date: 20110519

Package Information of Primidone

Package NDC: 50268-687-15
Package Description: 50 TABLET in 1 BOX, UNIT-DOSE (50268-687-15)

NDC Information of Primidone

NDC Code 50268-687-15
Proprietary Name Primidone
Package Description 50 TABLET in 1 BOX, UNIT-DOSE (50268-687-15)
Product NDC 50268-687
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110519
Marketing Category Name ANDA
Labeler Name AvPAK
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 Primidone


General Information