NDC 68382-092 – Carvedilol
Carvedilol 3.125 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-092
Product details
- Brand name
- Carvedilol
- Generic name
- Carvedilol
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077614
- Marketed since
- September 5, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- alpha-Adrenergic Blocker; beta-Adrenergic Blocker
Active ingredients
- Carvedilol 3.125 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68382-092-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-092-01) | Sep 5, 2007 |
| 68382-092-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-092-05) | Sep 5, 2007 |
| 68382-092-17 | 28 TABLET, FILM COATED in 1 BOTTLE (68382-092-17) | Sep 5, 2007 |
Recalls mentioning this NDC
- D-0753-2021 Aug 25, 2021 · Class II
Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were found in the bottle - D-1273-2019 May 15, 2019 · Class II
Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir Tablets USP 400 mg actually contained Carvedilol Tablets 6.25 mg - D-1242-2019 May 1, 2019 · Class III
Presence of Foreign Tablets/Capsules: Customer complaint for a small, solid, light yellow substance, identified as a fragmented tablet of another drug product, found mixed with tablets in a bottle of…
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