OXCARBAZEPINE
- Product NDC
- 63629-2075
- 11-digit product format
- 636292075
- Labeler code
- 63629
- Product ID
- 63629-2075_df7141ff-d76f-407d-ae81-578d14d5b66d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXCARBAZEPINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078069
- Marketing category
- ANDA
- Marketing start
- 2008-01-11
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2075 | OXCARBAZEPINE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 105 | Legacy NDC | 20240901_f8f85e08-5c1c-4a24-86d1-487954c27419.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2075-1 | 63629207501 | 500 TABLET, FILM COATED in 1 BOTTLE (63629-2075-1) | 2021-02-04 | 0000-00-00 | No | No | Current |