VALPROIC ACID
- Product NDC
- 71335-2250
- 11-digit product format
- 713352250
- Labeler code
- 71335
- Product ID
- 71335-2250_b150ac16-0468-489e-8305-80f6a6729f87
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VALPROIC ACID
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075379
- Marketing category
- ANDA
- Marketing start
- 2005-04-11
- 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 |
|---|
| 71335-2250-1 | VALPROIC ACID | 473 mL in 1 BOTTLE | SOLUTION | 473 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-2250 | VALPROIC ACID SOLUTION [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20241019_db53c5aa-d7a5-49ba-8227-c2d67ced23e2.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 |
|---|
| 71335-2250-1 | 71335225001 | 473 mL in 1 BOTTLE (71335-2250-1) | 473 ml | 2021-08-11 | No | No | Current |