NDC 23155-752 – Benazepril Hydrochloride
Benazepril Hydrochloride 40 mg/1 · Tablet · Oral
Product NDC23155-752
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- 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 40 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 23155-752-01 | 100 TABLET in 1 BOTTLE (23155-752-01) | Aug 20, 2022 |
| 23155-752-05 | 500 TABLET in 1 BOTTLE (23155-752-05) | Aug 20, 2022 |
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