Valproic Acid
- Product NDC
- 72603-253
- 11-digit product format
- 726030253
- Labeler code
- 72603
- Product ID
- 72603-253_1286acbf-3497-5aed-e063-6294a90af8be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- NorthStar Rx LLC
- Application
- ANDA073178
- Marketing category
- ANDA
- Marketing start
- 2024-06-10
- Substance
- VALPROIC ACID
- Active strength
- 250 mg/5mL
- 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 | 250 mg/5mL |
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 |
|---|
| 72603-253-01 | Valproic Acid | 473 mL in 1 BOTTLE | SOLUTION | 473 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72603-253 | VALPROIC ACID SOLUTION [NORTHSTAR RX LLC] | 1 | Current NDC, 1 package rows | 20240611_1286ab49-fa34-488e-e063-6394a90ad582.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-253-01 | 72603025301 | 473 mL in 1 BOTTLE (72603-253-01) | 473 ml | 2024-06-10 | No | No | Historical |