Oxcarbazepine
- Product NDC
- 70518-1073
- 11-digit product format
- 705181073
- Labeler code
- 70518
- Product ID
- 70518-1073_9010ed82-cd54-08b3-e053-2a95a90a83b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077794
- Marketing category
- ANDA
- Marketing start
- 2018-03-21
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record