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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 614OI1Z5WI | VALPROIC ACID | 99-66-1 | VALPROIC ACID |
Packages
| 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 | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| VALPROIC ACID | Bryant Ranch Prepack | 2024-10-04 | HUMAN PRESCRIPTION DRUG LABEL | 101 |