NDC 65862-117 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-117
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- 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 20 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 65862-117-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01) | May 22, 2008 |
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