oxcarbazepine
- Product NDC
- 70771-1842
- 11-digit product format
- 707711842
- Labeler code
- 70771
- Product ID
- 70771-1842_905fd0b0-fd53-48f5-83ff-129a5f5f104c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxcarbazepine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA211747
- Marketing category
- ANDA
- Marketing start
- 2025-07-10
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| VZI5B1W380 | OXCARBAZEPINE | 28721-07-5 | OXCARBAZEPINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1842-1 | 70771184201 | 100 TABLET in 1 BOTTLE (70771-1842-1) | 100 tablet | 2025-07-10 | No | No | Historical |
| 70771-1842-4 | 70771184204 | 10 BLISTER PACK in 1 CARTON (70771-1842-4) / 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2025-07-10 | No | No | Historical |
| 70771-1842-5 | 70771184205 | 500 TABLET in 1 BOTTLE (70771-1842-5) | 500 tablet | 2025-07-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| oxcarbazepine | Zydus Lifesciences Limited | 2025-10-10 | HUMAN PRESCRIPTION DRUG LABEL | 3 |
| oxcarbazepine | Zydus Lifesciences Limited | 2024-09-25 | HUMAN PRESCRIPTION DRUG LABEL | 2 |