NDC 31722-025 – Oxcarbazepine
Oxcarbazepine 600 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-025
Product details
- Brand name
- Oxcarbazepine
- Generic name
- Oxcarbazepine
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215939
- Marketed since
- January 11, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Oxcarbazepine 600 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 31722-025-01 | 100 TABLET, FILM COATED in 1 BOTTLE (31722-025-01) | Jan 11, 2022 |
| 31722-025-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-025-05) | Mar 10, 2023 |
| 31722-025-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (31722-025-10) | Mar 10, 2023 |
| 31722-025-31 | 10 BLISTER PACK in 1 CARTON (31722-025-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Jan 11, 2022 |
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