NDC 0143-9785 – Valproate Sodium
Valproate Sodium 500 mg/5mL · Injection · Intravenous
Product NDC0143-9785
Product details
- Brand name
- Valproate Sodium
- Generic name
- Valproate Sodium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection
- Route
- Intravenous
- Marketing category
- ANDA · ANDA078523
- Marketed since
- February 17, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Valproate Sodium 500 mg/5mL
Uses, dosage, side effects and warnings for Valproate Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9785-10 | 10 VIAL, SINGLE-DOSE in 1 CARTON (0143-9785-10) / 5 mL in 1 VIAL, SINGLE-DOSE (0143-9785-01) | Feb 17, 2010 |