NDC 68382-022 – Atenolol
Atenolol 25 mg/1 · Tablet · Oral
Product NDC68382-022
Product details
- Brand name
- Atenolol
- Generic name
- Atenolol
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076900
- Marketed since
- October 8, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Atenolol 25 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68382-022-01 | 100 TABLET in 1 BOTTLE (68382-022-01) | Oct 8, 2005 |
| 68382-022-10 | 1000 TABLET in 1 BOTTLE (68382-022-10) | Oct 8, 2005 |
| 68382-022-16 | 90 TABLET in 1 BOTTLE (68382-022-16) | Oct 8, 2005 |
| 68382-022-24 | 10000 TABLET in 1 BOTTLE (68382-022-24) | Oct 8, 2005 |
| 68382-022-40 | 5000 TABLET in 1 BOTTLE (68382-022-40) | Oct 8, 2005 |
Recalls mentioning this NDC
- D-0605-2017 Mar 29, 2017 · Class II
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet. - D-0007-2015 Oct 15, 2014 · Class II
Superpotent Drug: A complaint was reported by a pharmacist who stated several tablets were noticeably thicker in appearance.
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