Oxcarbazepine
- Product NDC
- 70518-1842
- 11-digit product format
- 705181842
- Labeler code
- 70518
- Product ID
- 70518-1842_f1db72e1-5b86-3dd4-e053-2a95a90af4ea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxcarbazepine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077794
- Marketing category
- ANDA
- Marketing start
- 2019-02-01
- 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
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1842 | OXCARBAZEPINE TABLET, FILM COATED [REMEDYREPACK INC.] | 11 | Legacy NDC | 20250302_d4737be8-7c17-4548-b380-808c5b4ad7ac.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1842-1 | 70518184201 | 100 POUCH in 1 BOX (70518-1842-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-1842-2) | 100 pouch | 2021-09-20 | 0000-00-00 | No | No | Current |
| 70518-1842-3 | 70518184203 | 100 POUCH in 1 BOX (70518-1842-3) > 1 TABLET, FILM COATED in 1 POUCH (70518-1842-4) | 100 pouch | 2023-01-07 | 0000-00-00 | No | No | Current |