NDC 43547-337 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC43547-337
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Solco healthcare U.S., LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- January 1, 2014
- Listing expires
- December 31, 2026
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 43547-337-03 | 30 TABLET, COATED in 1 BOTTLE (43547-337-03) | Jun 30, 2019 |
| 43547-337-10 | 100 TABLET, COATED in 1 BOTTLE (43547-337-10) | Jan 1, 2014 |
| 43547-337-50 | 500 TABLET, COATED in 1 BOTTLE (43547-337-50) | Jan 1, 2014 |
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