NDC 65162-752 – Benazepril Hydrochloride
Benazepril Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC65162-752
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076820
- Marketed since
- February 2, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 65162-752-03 | 30 TABLET in 1 BOTTLE (65162-752-03) | Feb 2, 2010 |
| 65162-752-10 | 100 TABLET in 1 BOTTLE (65162-752-10) | Feb 2, 2010 |
| 65162-752-50 | 500 TABLET in 1 BOTTLE (65162-752-50) | Feb 2, 2010 |
Recalls mentioning this NDC
- D-0134-2020 Oct 16, 2019 · Class III
Presence of Foreign Tablet/Capsule; Promethazine HCl tablet found in the Benazepril HCl bottle
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