Oxcarbazepine
- Product NDC
- 72189-573
- 11-digit product format
- 721890573
- Labeler code
- 72189
- Product ID
- 72189-573_21b0cc84-b64b-75de-e063-6294a90a9dd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_rx
- Application
- ANDA077802
- Marketing category
- ANDA
- Marketing start
- 2024-09-09
- Substance
- OXCARBAZEPINE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VZI5B1W380 | OXCARBAZEPINE | 28721-07-5 | OXCARBAZEPINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-573-60 | 72189057360 | 60 TABLET, FILM COATED in 1 BOTTLE (72189-573-60) | 2024-09-09 | No | No | Historical |