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Valproic Acid - 62756-873-08 - (Valproic Acid)

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Drug Information of Valproic Acid

Product NDC: 62756-873
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
Coding System: National Drug Codes(NDC)

Labeler Information of Valproic Acid

Product NDC: 62756-873
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091037
Marketing Category: ANDA
Start Marketing Date: 20130228

Package Information of Valproic Acid

Package NDC: 62756-873-08
Package Description: 100 CAPSULE in 1 BOTTLE (62756-873-08)

NDC Information of Valproic Acid

NDC Code 62756-873-08
Proprietary Name Valproic Acid
Package Description 100 CAPSULE in 1 BOTTLE (62756-873-08)
Product NDC 62756-873
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Valproic Acid
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130228
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
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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