NDC 51407-464 – Benazepril Hydrochloride
Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · Oral
Product NDC51407-464
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Golden State Medical Supply, Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- February 11, 2004
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 51407-464-01 | 100 TABLET, COATED in 1 BOTTLE (51407-464-01) | Jul 6, 2021 |
| 51407-464-05 | 500 TABLET, COATED in 1 BOTTLE (51407-464-05) | Jul 6, 2021 |
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