NDC 62135-721 – Benazepril hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC62135-721
Product details
- Brand name
- Benazepril hydrochloride
- Generic name
- Benazepril hydrochloride
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076267
- Marketed since
- August 20, 2022
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 62135-721-90 | 90 TABLET in 1 BOTTLE (62135-721-90) | Jul 20, 2023 |
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