Oxcarbazepine
- Product NDC
- 0054-0199
- 11-digit product format
- 000540199
- Labeler code
- 0054
- Product ID
- 0054-0199_5656afa9-bc76-4583-aa0b-95af5cb0b15a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- West-Ward Pharmaceuticals Corp.
- Application
- ANDA201193
- Marketing category
- ANDA
- Marketing start
- 2012-10-03
- Marketing end
- 0000-00-00
- Substance
- OXCARBAZEPINE
- Active strength
- 300 mg/5mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 0054-0199-59 | 00054019959 | 250 mL in 1 BOTTLE (0054-0199-59) | 250 ml | 2012-10-03 | 0000-00-00 | No | No | Current |