NDC 62756-183 – Oxcarbazepine
Oxcarbazepine 150 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-183
Product details
- Brand name
- Oxcarbazepine
- Generic name
- Oxcarbazepine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077794
- Marketed since
- October 9, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Oxcarbazepine 150 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62756-183-08 | 100 TABLET, FILM COATED in 1 BOTTLE (62756-183-08) | Oct 9, 2007 |
| 62756-183-83 | 30 TABLET, FILM COATED in 1 BOTTLE (62756-183-83) | Oct 9, 2007 |
Recalls mentioning this NDC
- D-0085-2023 Dec 28, 2022 · Class II
Presence of foreign substance - D-1081-2014 Feb 19, 2014 · Class II
Failed Tablet Specifications: Broken Tablets Present.
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