NDC 65862-142 – Carvedilol
Carvedilol 3.125 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-142
Product details
- Brand name
- Carvedilol
- Generic name
- Carvedilol
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078332
- Marketed since
- September 5, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- alpha-Adrenergic Blocker; beta-Adrenergic Blocker
Active ingredients
- Carvedilol 3.125 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65862-142-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-142-01) | Sep 5, 2007 |
| 65862-142-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-142-05) | Sep 5, 2007 |
| 65862-142-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-142-99) | Sep 5, 2007 |
Recalls mentioning this NDC
- D-0263-2022 Dec 1, 2021 · Class III
Failed Impurities/Degradation Specifications
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