NDC 0143-9785
Valproate Sodium
Valproate Sodium
Valproate Sodium is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by West-ward Pharmaceuticals Corp. The primary component is Valproate Sodium.
| Product ID | 0143-9785_4984517f-702b-4547-bea2-e5a10f397431 |
| NDC | 0143-9785 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Valproate Sodium |
| Generic Name | Valproate Sodium |
| Dosage Form | Injection |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2010-02-17 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA078523 |
| Labeler Name | West-Ward Pharmaceuticals Corp |
| Substance Name | VALPROATE SODIUM |
| Active Ingredient Strength | 500 mg/5mL |
| Pharm Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |