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