Valproic Acid
- Product NDC
- 68999-874
- 11-digit product format
- 689990874
- Labeler code
- 68999
- Product ID
- 68999-874_43f6119e-621e-ca3f-e063-6394a90a562e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Chartwell Governmental & Specialty RX, LLC.
- Application
- ANDA075782
- Marketing category
- ANDA
- Marketing start
- 2000-12-22
- Substance
- VALPROIC ACID
- Active strength
- 500 mg/10mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Valproic Acid
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VALPROIC ACID | 500 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 614OI1Z5WI |
| Rxcui | 1099687 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68999-874-24 | Valproic Acid | 2 in 1 BOX | SOLUTION | 2 | | 1 |
| 68999-874-24 | Valproic Acid | 10 in 1 TRAY | SOLUTION | 10 | | 1 |
| 68999-874-59 | Valproic Acid | 10 mL in 1 CUP | SOLUTION | 10 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68999-874-24 | 68999087424 | 2 TRAY in 1 BOX (68999-874-24) / 10 CUP in 1 TRAY / 10 mL in 1 CUP (68999-874-59) | 2 tray | 2025-11-14 | No | No | Historical |
| 68999-874-59 | 68999087459 | 10 mL in 1 CUP | 10 ml | | | | Historical |