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Valproic Acid
Valproic Acid - 0121-4675-05 - (VALPROIC ACID)
Drug Information of Valproic Acid
| Product NDC: | 0121-4675 |
| 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: | 0121-4675 |
| Labeler Name: | Pharmaceutical Associates, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075379 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050411 |
Package Information of Valproic Acid
| Package NDC: | 0121-4675-05 |
| Package Description: | 4 TRAY in 1 CASE (0121-4675-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
NDC Information of Valproic Acid
| NDC Code | 0121-4675-05 |
| Proprietary Name | Valproic Acid |
| Package Description | 4 TRAY in 1 CASE (0121-4675-05) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 0121-4675 |
| 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 | Pharmaceutical Associates, Inc. |
| 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] |
