Valproic acid
- Product NDC
- 71930-057
- 11-digit product format
- 719300057
- Labeler code
- 71930
- Product ID
- 71930-057_052dbbdb-4a8d-4a7b-a601-0edef0d2ab7a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic acid
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Eywa Pharma Inc
- Application
- ANDA207611
- Marketing category
- ANDA
- Marketing start
- 2020-02-21
- Marketing end
- 0000-00-00
- Substance
- VALPROIC ACID
- Active strength
- 250 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71930-057-12 | 71930005712 | 100 CAPSULE in 1 BOTTLE (71930-057-12) | 100 capsule | 2020-02-21 | 0000-00-00 | No | No | Current |