Valproic Acid
- Product NDC
- 60687-262
- 11-digit product format
- 606870262
- Labeler code
- 60687
- Product ID
- 60687-262_e7892073-a56b-5f17-e053-2995a90a4cf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA070868
- Marketing category
- ANDA
- Marketing start
- 2019-10-17
- Marketing end
- 2024-01-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-262-56 | 60687026256 | 10 TRAY in 1 CASE (60687-262-56) > 10 CUP, UNIT-DOSE in 1 TRAY (60687-262-48) > 10 mL in 1 CUP, UNIT-DOSE (60687-262-42) | 10 tray | 2019-10-17 | 0000-00-00 | No | No | Current |