NDC 62559-524 – Benazepril Hydrochloride
Benazepril Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC62559-524
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- ANI Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076333
- Marketed since
- July 27, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 62559-524-01 | 100 TABLET in 1 BOTTLE (62559-524-01) | Jul 27, 2026 |
| 62559-524-05 | 500 TABLET in 1 BOTTLE (62559-524-05) | Jul 27, 2026 |
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