PRIMIDONE - 42549-680-30 - (PRIMIDONE)

Alphabetical Index


Drug Information of PRIMIDONE

Product NDC: 42549-680
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: 42549-680
Labeler Name: STAT Rx USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084903
Marketing Category: ANDA
Start Marketing Date: 20010524

Package Information of PRIMIDONE

Package NDC: 42549-680-30
Package Description: 30 TABLET in 1 BOTTLE (42549-680-30)

NDC Information of PRIMIDONE

NDC Code 42549-680-30
Proprietary Name PRIMIDONE
Package Description 30 TABLET in 1 BOTTLE (42549-680-30)
Product NDC 42549-680
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PRIMIDONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010524
Marketing Category Name ANDA
Labeler Name STAT Rx USA LLC
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