Oxcarbazepine
- Product NDC
- 71335-0144
- 11-digit product format
- 713350144
- Labeler code
- 71335
- Product ID
- 71335-0144_1a89b1ea-fb13-4e73-aa35-46da5bc09c30
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077802
- Marketing category
- ANDA
- Marketing start
- 2007-10-09
- Marketing end
- 0000-00-00
- Substance
- OXCARBAZEPINE
- Active strength
- 600 mg/1
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0144-1 | 71335014401 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0144-1) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0144-2 | 71335014402 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0144-2) | 2021-12-27 | 0000-00-00 | No | No | Current |
| 71335-0144-3 | 71335014403 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0144-3) | 2021-12-27 | 0000-00-00 | No | No | Current |