Primidone - 0115-1030-02 - (PRIMIDONE)

Alphabetical Index


Drug Information of Primidone

Product NDC: 0115-1030
Proprietary Name: Primidone
Non Proprietary Name: PRIMIDONE
Active Ingredient(s): 50    mg/1 & nbsp;   PRIMIDONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Primidone

Product NDC: 0115-1030
Labeler Name: Global Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040717
Marketing Category: ANDA
Start Marketing Date: 20080212

Package Information of Primidone

Package NDC: 0115-1030-02
Package Description: 500 TABLET in 1 BOTTLE (0115-1030-02)

NDC Information of Primidone

NDC Code 0115-1030-02
Proprietary Name Primidone
Package Description 500 TABLET in 1 BOTTLE (0115-1030-02)
Product NDC 0115-1030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRIMIDONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080212
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals
Substance Name PRIMIDONE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of Primidone


General Information