NDC 70518-4633 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC70518-4633
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076267
- Marketed since
- April 25, 2026
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 70518-4633-0 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-4633-0) | Apr 25, 2026 |
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