NDC 51672-4005 – Carbamazepine
Carbamazepine 200 mg/1 · Tablet · Oral
Product NDC51672-4005
Product details
- Brand name
- Carbamazepine
- Generic name
- Carbamazepine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074649
- Marketed since
- October 3, 1996
- Listing expires
- December 31, 2027
- Pharmacologic class
- Mood Stabilizer
Active ingredients
- Carbamazepine 200 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 51672-4005-1 | 100 TABLET in 1 BOTTLE (51672-4005-1) | Oct 3, 1996 |
| 51672-4005-2 | 500 TABLET in 1 BOTTLE (51672-4005-2) | Oct 3, 1996 |
| 51672-4005-3 | 1000 TABLET in 1 BOTTLE (51672-4005-3) | Oct 3, 1996 |
Recalls mentioning this NDC
- D-0770-2026 Aug 26, 2026 · Class II
CGMP Deviations; black spots found on tablets from burnt excipient during manufacturing - D-0049-2015 Nov 5, 2014 · Class III
Marketed without an Approved NDA/ANDA: One lot was on hold-pending release status when it was erroneously made available for sale in the inventory control system. An alternate manufacturing site for…
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