NDC 71335-1365 – Benazepril Hydrochloride
Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1365
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078212
- Marketed since
- May 22, 2008
- Marketing end
- November 30, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1365-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1) | Feb 13, 2020 |
| 71335-1365-2 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2) | Oct 7, 2019 |
| 71335-1365-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3) | May 30, 2024 |
| 71335-1365-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4) | Mar 11, 2020 |
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