NDC 68788-6957 – Benazepril Hydrochloride
Benazepril Hydrochloride 40 mg/1 · Tablet, Coated · Oral
Product NDC68788-6957
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- May 2, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 40 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-6957-1 | 100 TABLET, COATED in 1 BOTTLE (68788-6957-1) | May 2, 2017 |
| 68788-6957-3 | 30 TABLET, COATED in 1 BOTTLE (68788-6957-3) | May 2, 2017 |
| 68788-6957-6 | 60 TABLET, COATED in 1 BOTTLE (68788-6957-6) | May 2, 2017 |
| 68788-6957-8 | 120 TABLET, COATED in 1 BOTTLE (68788-6957-8) | May 2, 2017 |
| 68788-6957-9 | 90 TABLET, COATED in 1 BOTTLE (68788-6957-9) | May 2, 2017 |
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