NDC 0116-4021 – Valproic Acid
Valproic Acid 250 mg/5mL · Solution · Oral
Product NDC0116-4021
Product details
- Brand name
- Valproic Acid
- Generic name
- Valproic Acid
- Labeler
- Xttrium Laboratories Inc.
- Dosage form
- Solution
- Route
- Oral
- Marketing category
- ANDA · ANDA070868
- Marketed since
- July 1, 1986
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Valproic Acid 250 mg/5mL
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 0116-4021-11 | 10 TRAY in 1 CASE (0116-4021-11) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4021-10) | Jul 29, 2025 |
| 0116-4021-16 | 473 mL in 1 BOTTLE, PLASTIC (0116-4021-16) | Jul 29, 2025 |
| 0116-4021-40 | 4 TRAY in 1 CASE (0116-4021-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05) | Jul 29, 2025 |
| 0116-4021-41 | 10 TRAY in 1 CASE (0116-4021-41) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0116-4021-05) | Jul 29, 2025 |
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