NDC 72162-2328 – Benazepril hydrochloride and hydrochlorothiazide
Benazepril Hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC72162-2328
Product details
- Brand name
- Benazepril hydrochloride and hydrochlorothiazide
- Generic name
- Benazepril hydrochloride and hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA020033
- Marketed since
- April 7, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Benazepril Hydrochloride 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Benazepril hydrochloride and hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-2328-1 | 100 TABLET in 1 BOTTLE (72162-2328-1) | Jun 18, 2024 |
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