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Valproic Acid - 55154-5361-0 - (Valproic Acid)

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Drug Information of Valproic Acid

Product NDC: 55154-5361
Proprietary Name: Valproic Acid
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 Acid

Product NDC: 55154-5361
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073229
Marketing Category: ANDA
Start Marketing Date: 20100604

Package Information of Valproic Acid

Package NDC: 55154-5361-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5361-0) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Valproic Acid

NDC Code 55154-5361-0
Proprietary Name Valproic Acid
Package Description 10 BLISTER PACK in 1 BAG (55154-5361-0) > 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 55154-5361
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valproic Acid
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100604
Marketing Category Name ANDA
Labeler Name Cardinal Health
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 Acid


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