NDC 51991-054 – Oxcarbazepine
Oxcarbazepine 300 mg/1 · Tablet, Film Coated · Oral
Product NDC51991-054
Product details
- Brand name
- Oxcarbazepine
- Generic name
- Oxcarbazepine
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078069
- Marketed since
- January 11, 2008
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Oxcarbazepine 300 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 51991-054-01 | 100 TABLET, FILM COATED in 1 BOTTLE (51991-054-01) | Jan 29, 2025 |
| 51991-054-05 | 500 TABLET, FILM COATED in 1 BOTTLE (51991-054-05) | Jan 29, 2025 |
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