Oxcarbazepine
- Product NDC
- 70518-2946
- 11-digit product format
- 705182946
- Labeler code
- 70518
- Product ID
- 70518-2946_dd296710-bc4b-7ffa-e053-2a95a90aaa73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202961
- Marketing category
- ANDA
- Marketing start
- 2020-11-24
- Marketing end
- 0000-00-00
- Substance
- OXCARBAZEPINE
- Active strength
- 300 mg/5mL
- 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 |
|---|
| 70518-2946-0 | 70518294600 | 10 CUP, UNIT-DOSE in 1 BOX (70518-2946-0) > 5 mL in 1 CUP, UNIT-DOSE (70518-2946-1) | | 2020-11-24 | 0000-00-00 | No | No | Current |
| 70518-2946-2 | 70518294602 | 10 mL in 1 CUP, UNIT-DOSE (70518-2946-2) | 10 ml | 2020-11-24 | 0000-00-00 | No | No | Current |
| 70518-2946-3 | 70518294603 | 7.5 mL in 1 CUP, UNIT-DOSE (70518-2946-3) | 7.5 ml | 2020-11-24 | 0000-00-00 | No | No | Current |