Oxcarbazepine
- Product NDC
- 68084-853
- 11-digit product format
- 680840853
- Labeler code
- 68084
- Product ID
- 68084-853_ea3fda1e-efeb-6d95-e053-2995a90adada
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA078069
- Marketing category
- ANDA
- Marketing start
- 2014-11-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-853-01 | 68084085301 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-853-01) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-853-11) | 100 blister pack | 2014-11-05 | 0000-00-00 | No | No | Current |