Oxcarbazepine
- Product NDC
- 63629-4987
- 11-digit product format
- 636294987
- Labeler code
- 63629
- Product ID
- 63629-4987_9530c23e-7f67-492c-b00c-a17092a5387e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077794
- Marketing category
- ANDA
- Marketing start
- 2007-10-09
- Marketing end
- 0000-00-00
- Substance
- OXCARBAZEPINE
- Active strength
- 300 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-4987-1 | 63629498701 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-4987-1) | 2013-04-18 | 0000-00-00 | No | No | Current |
| 63629-4987-2 | 63629498702 | 60 TABLET, FILM COATED in 1 BOTTLE (63629-4987-2) | 2013-04-18 | 0000-00-00 | No | No | Current |
| 63629-4987-3 | 63629498703 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-4987-3) | 2013-04-18 | 0000-00-00 | No | No | Current |
| 63629-4987-4 | 63629498704 | 180 TABLET, FILM COATED in 1 BOTTLE (63629-4987-4) | 2013-04-18 | 0000-00-00 | No | No | Current |
| 63629-4987-5 | 63629498705 | 120 TABLET, FILM COATED in 1 BOTTLE (63629-4987-5) | 2022-02-02 | 0000-00-00 | No | No | Current |