NDC 71205-320 – Benazepril Hydrochloride
Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-320
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078212
- Marketed since
- May 22, 2008
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 71205-320-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30) | Sep 1, 2019 |
| 71205-320-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60) | Sep 1, 2019 |
| 71205-320-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90) | Sep 1, 2019 |
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