Oxcarbazepine
- Product NDC
- 55154-8187
- 11-digit product format
- 551548187
- Labeler code
- 55154
- Product ID
- 55154-8187_3bc13938-b3d4-43db-a0af-741413e5846c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA078069
- Marketing category
- ANDA
- Marketing start
- 2014-11-04
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 55154-8187-0 | 55154818700 | 10 BLISTER PACK in 1 BAG (55154-8187-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 10 blister pack | 2014-11-04 | 0000-00-00 | No | No | Current |