NDC 0904-7308 – Carvedilol
Carvedilol 25 mg/1 · Tablet, Film Coated · Oral
Product NDC0904-7308
Product details
- Brand name
- Carvedilol
- Generic name
- Carvedilol
- Labeler
- Major Pharmaceuticals
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078251
- Marketed since
- July 1, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- alpha-Adrenergic Blocker; beta-Adrenergic Blocker
Active ingredients
- Carvedilol 25 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0904-7308-61 | 100 BLISTER PACK in 1 CARTON (0904-7308-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK | Jul 1, 2024 |
Recalls mentioning this NDC
- D-0594-2025 Aug 27, 2025 · Class II
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
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