Home
>
National Drug Code (NDC)
>
Valproic Acid
Valproic Acid - 0603-1841-56 - (Valproic Acid)
Drug Information of Valproic Acid
| Product NDC: | 0603-1841 |
| 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: | 0603-1841 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077960 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061013 |
Package Information of Valproic Acid
| Package NDC: | 0603-1841-56 |
| Package Description: | 237 mL in 1 BOTTLE (0603-1841-56) |
NDC Information of Valproic Acid
| NDC Code | 0603-1841-56 |
| Proprietary Name | Valproic Acid |
| Package Description | 237 mL in 1 BOTTLE (0603-1841-56) |
| Product NDC | 0603-1841 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Valproic Acid |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20061013 |
| Marketing Category Name | ANDA |
| Labeler Name | Qualitest Pharmaceuticals |
| 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] |
