Valproic - 54868-1689-2 - (Valproic Acid)

Alphabetical Index


Drug Information of Valproic

Product NDC: 54868-1689
Proprietary Name: Valproic
Non Proprietary Name: Valproic Acid
Active Ingredient(s): 250    mg/1 & nbsp;   Valproic Acid
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Valproic

Product NDC: 54868-1689
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073229
Marketing Category: ANDA
Start Marketing Date: 19940419

Package Information of Valproic

Package NDC: 54868-1689-2
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-1689-2)

NDC Information of Valproic

NDC Code 54868-1689-2
Proprietary Name Valproic
Package Description 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (54868-1689-2)
Product NDC 54868-1689
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valproic Acid
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 19940419
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name VALPROIC ACID
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]

Complete Information of Valproic


General Information