Benazepril Hydrochloride
- Product NDC
- 72162-1816
- 11-digit product format
- 721621816
- Labeler code
- 72162
- Product ID
- 72162-1816_ea0f1205-c572-429b-ae69-01e6b88a1075
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076820
- Marketing category
- ANDA
- Marketing start
- 2010-02-02
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| N1SN99T69T | BENAZEPRIL HYDROCHLORIDE | 86541-74-4 | BENAZEPRIL HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1816-3 | 72162181603 | 30 TABLET in 1 BOTTLE (72162-1816-3) | 30 tablet | 2023-05-08 | No | No | Historical |
| 72162-1816-9 | 72162181609 | 90 TABLET in 1 BOTTLE (72162-1816-9) | 90 tablet | 2023-05-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Benazepril Hydrochloride | Bryant Ranch Prepack | 2023-05-08 | HUMAN PRESCRIPTION DRUG LABEL | 100 |