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Valproic Acid - 55154-9430-5 - (VALPROIC ACID)

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Drug Information of Valproic Acid

Product NDC: 55154-9430
Proprietary Name: Valproic Acid
Non Proprietary Name: VALPROIC ACID
Active Ingredient(s): 250    mg/5mL & nbsp;   VALPROIC ACID
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Valproic Acid

Product NDC: 55154-9430
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075379
Marketing Category: ANDA
Start Marketing Date: 20050411

Package Information of Valproic Acid

Package NDC: 55154-9430-5
Package Description: 5 CUP, UNIT-DOSE in 1 BAG (55154-9430-5) > 5 mL in 1 CUP, UNIT-DOSE

NDC Information of Valproic Acid

NDC Code 55154-9430-5
Proprietary Name Valproic Acid
Package Description 5 CUP, UNIT-DOSE in 1 BAG (55154-9430-5) > 5 mL in 1 CUP, UNIT-DOSE
Product NDC 55154-9430
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VALPROIC ACID
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20050411
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name VALPROIC ACID
Strength Number 250
Strength Unit mg/5mL
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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