NDC 68462-578 – Benazepril Hydrochloride and Hydrochlorothiazide
Benazepril Hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-578
Product details
- Brand name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Generic name
- Benazepril Hydrochloride and Hydrochlorothiazide
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076631
- Marketed since
- February 11, 2004
- 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 |
|---|---|---|
| 68462-578-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68462-578-01) | Nov 30, 2023 |
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