Primidone - 55111-477-78 - (Primidone)

Alphabetical Index


Drug Information of Primidone

Product NDC: 55111-477
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: 55111-477
Labeler Name: Dr. Reddy's Laboratories Ltd
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040862
Marketing Category: ANDA
Start Marketing Date: 20081003

Package Information of Primidone

Package NDC: 55111-477-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-477-78) > 10 TABLET in 1 BLISTER PACK (55111-477-79)

NDC Information of Primidone

NDC Code 55111-477-78
Proprietary Name Primidone
Package Description 10 BLISTER PACK in 1 CARTON (55111-477-78) > 10 TABLET in 1 BLISTER PACK (55111-477-79)
Product NDC 55111-477
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Primidone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081003
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Ltd
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