NDC 71205-244 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC71205-244
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Proficient Rx LP
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-244-30 | 30 TABLET in 1 BOTTLE (71205-244-30) | Mar 1, 2019 |
| 71205-244-60 | 60 TABLET in 1 BOTTLE (71205-244-60) | Mar 1, 2019 |
| 71205-244-90 | 90 TABLET in 1 BOTTLE (71205-244-90) | Mar 1, 2019 |
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