NDC 50090-3243 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC50090-3243
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- January 1, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50090-3243-0 | 30 TABLET, COATED in 1 BOTTLE (50090-3243-0) | Nov 17, 2017 |
| 50090-3243-1 | 90 TABLET, COATED in 1 BOTTLE (50090-3243-1) | Nov 3, 2017 |
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