NDC 68788-7866 – Oxcarbazepine
Oxcarbazepine 600 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-7866
Product details
- Brand name
- Oxcarbazepine
- Generic name
- Oxcarbazepine
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078069
- Marketed since
- February 15, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Oxcarbazepine 600 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7866-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7866-3) | Feb 15, 2021 |
| 68788-7866-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7866-6) | Feb 15, 2021 |
| 68788-7866-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7866-9) | Feb 15, 2021 |
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