NDC 71335-0854 – Benazepril Hydrochloride
Benazepril Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC71335-0854
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0854-1 | 30 TABLET in 1 BOTTLE (71335-0854-1) | Aug 17, 2018 |
| 71335-0854-2 | 60 TABLET in 1 BOTTLE (71335-0854-2) | Mar 9, 2022 |
| 71335-0854-3 | 100 TABLET in 1 BOTTLE (71335-0854-3) | Apr 11, 2022 |
| 71335-0854-4 | 90 TABLET in 1 BOTTLE (71335-0854-4) | Jun 11, 2018 |
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