Primidone - 42291-511-50 - (Primidone)

Alphabetical Index


Drug Information of Primidone

Product NDC: 42291-511
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: 42291-511
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040866
Marketing Category: ANDA
Start Marketing Date: 20080424

Package Information of Primidone

Package NDC: 42291-511-50
Package Description: 500 TABLET in 1 BOTTLE (42291-511-50)

NDC Information of Primidone

NDC Code 42291-511-50
Proprietary Name Primidone
Package Description 500 TABLET in 1 BOTTLE (42291-511-50)
Product NDC 42291-511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080424
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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