NDC 51655-066 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC51655-066
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- March 4, 2016
- 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 |
|---|---|---|
| 51655-066-26 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-066-26) | Jul 11, 2022 |
| 51655-066-52 | 30 TABLET, COATED in 1 BOTTLE, DISPENSING (51655-066-52) | Mar 4, 2016 |
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