Oxcarbazepine
- Product NDC
- 70518-0111
- 11-digit product format
- 705180111
- Labeler code
- 70518
- Product ID
- 70518-0111_809ca60e-5d49-d4de-e053-2991aa0ab616
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077795
- Marketing category
- ANDA
- Marketing start
- 2017-01-10
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record