Primidone - 54868-1691-3 - (Primidone)

Alphabetical Index


Drug Information of Primidone

Product NDC: 54868-1691
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: 54868-1691
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084903
Marketing Category: ANDA
Start Marketing Date: 20090727

Package Information of Primidone

Package NDC: 54868-1691-3
Package Description: 100 TABLET in 1 BOTTLE (54868-1691-3)

NDC Information of Primidone

NDC Code 54868-1691-3
Proprietary Name Primidone
Package Description 100 TABLET in 1 BOTTLE (54868-1691-3)
Product NDC 54868-1691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090727
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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