Benazepril Hydrochloride
- Product NDC
- 71205-244
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076820
- Marketing category
- ANDA
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-244-30 | 30 TABLET in 1 BOTTLE (71205-244-30) | 2019-03-01 | | No | Historical |
| 71205-244-60 | 60 TABLET in 1 BOTTLE (71205-244-60) | 2019-03-01 | | No | Historical |
| 71205-244-90 | 90 TABLET in 1 BOTTLE (71205-244-90) | 2019-03-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Benazepril Hydrochloride | Proficient Rx LP | 2019-10-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |