NDC 50090-3359 – Benazepril Hydrochloride
Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Oral
Product NDC50090-3359
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- A-S Medication Solutions
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-3359-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0) | Mar 26, 2018 |
| 50090-3359-1 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1) | Feb 2, 2018 |
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