NDC 50268-109 – Benazepril Hydrochloride
Benazepril Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC50268-109
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- AvPAK
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076820
- Marketed since
- April 28, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50268-109-15 | 50 BLISTER PACK in 1 BOX (50268-109-15) / 1 TABLET in 1 BLISTER PACK (50268-109-11) | Apr 28, 2014 |
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