NDC 71335-0078 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC71335-0078
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- January 1, 2014
- 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 |
|---|---|---|
| 71335-0078-1 | 30 TABLET, COATED in 1 BOTTLE (71335-0078-1) | Feb 9, 2022 |
| 71335-0078-2 | 60 TABLET, COATED in 1 BOTTLE (71335-0078-2) | Feb 9, 2022 |
| 71335-0078-3 | 100 TABLET, COATED in 1 BOTTLE (71335-0078-3) | Feb 9, 2022 |
| 71335-0078-4 | 90 TABLET, COATED in 1 BOTTLE (71335-0078-4) | Feb 9, 2022 |
| 71335-0078-5 | 14 TABLET, COATED in 1 BOTTLE (71335-0078-5) | Feb 9, 2022 |
| 71335-0078-6 | 10 TABLET, COATED in 1 BOTTLE (71335-0078-6) | Feb 9, 2022 |
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