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Valproic
Valproic - 0591-4012-01 - (Valproic Acid)
Drug Information of Valproic
| Product NDC: | 0591-4012 |
| Proprietary Name: | Valproic |
| Non Proprietary Name: | Valproic Acid |
| Active Ingredient(s): | 250 mg/1 & nbsp; Valproic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Valproic
| Product NDC: | 0591-4012 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073229 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090908 |
Package Information of Valproic
| Package NDC: | 0591-4012-01 |
| Package Description: | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0591-4012-01) |
NDC Information of Valproic
| NDC Code | 0591-4012-01 |
| Proprietary Name | Valproic |
| Package Description | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0591-4012-01) |
| Product NDC | 0591-4012 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Valproic Acid |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20090908 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| 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] |
