NDC 51655-388 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-388
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078212
- Marketed since
- May 19, 2023
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 51655-388-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-388-52) | May 19, 2023 |
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