NDC 51655-202 – Benazepril Hydrochloride
Benazepril Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-202
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
- March 15, 2023
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 51655-202-26 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26) | Mar 15, 2023 |
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
- 50090-3359 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 65862-117 Benazepril Hydrochloride 20 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 65862-118 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 84386-102 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 84386-101 Benazepril Hydrochloride 20 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 84386-100 Benazepril Hydrochloride 10 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 71335-1365 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 51655-388 Benazepril Hydrochloride 20 mg/1 · Tablet, Film Coated · Northwind Health Company, LLC
- 51655-617 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · Northwind Health Company, LLC
- 68071-5028 Benazepril Hydrochloride 40 mg/1 · Tablet, Film Coated · NuCare Pharmaceuticals,Inc.