NDC 68071-5129 – Benazepril Hydrochloride
Benazepril Hydrochloride 10 mg/1 · Tablet, Coated · Oral
Product NDC68071-5129
Product details
- Brand name
- Benazepril Hydrochloride
- Generic name
- Benazepril Hydrochloride
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076118
- Marketed since
- January 1, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Benazepril Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68071-5129-1 | 100 TABLET, COATED in 1 BOTTLE (68071-5129-1) | Dec 11, 2019 |
Other Benazepril Hydrochloride products
- 50090-5751 Benazepril Hydrochloride 10 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-5750 Benazepril Hydrochloride 20 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-3775 Benazepril Hydrochloride 10 mg/1 · Tablet, Coated · A-S Medication Solutions
- 50090-3359 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-0914 Benazepril Hydrochloride 40 mg/1 · Tablet, Coated · A-S Medication Solutions
- 50090-3243 Benazepril Hydrochloride 20 mg/1 · Tablet, Coated · A-S Medication Solutions
- 65162-753 Benazepril Hydrochloride 20 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 65162-754 Benazepril Hydrochloride 40 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 65162-752 Benazepril Hydrochloride 10 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 65162-751 Benazepril Hydrochloride 5 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 53746-753 Benazepril Hydrochloride 20 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 53746-752 Benazepril Hydrochloride 10 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC