NDC 71335-1086 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71335-1086
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 20 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1086-1 | 30 TABLET in 1 BOTTLE (71335-1086-1) | May 4, 2022 |
| 71335-1086-2 | 60 TABLET in 1 BOTTLE (71335-1086-2) | May 4, 2022 |
| 71335-1086-3 | 100 TABLET in 1 BOTTLE (71335-1086-3) | May 4, 2022 |
| 71335-1086-4 | 90 TABLET in 1 BOTTLE (71335-1086-4) | May 4, 2022 |
| 71335-1086-5 | 14 TABLET in 1 BOTTLE (71335-1086-5) | May 4, 2022 |
| 71335-1086-6 | 10 TABLET in 1 BOTTLE (71335-1086-6) | May 4, 2022 |
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