Benazepril Hydrochloride
- Product NDC
- 63187-499
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076118
- Marketing category
- ANDA
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 63187-499-30 | 30 TABLET, COATED in 1 BOTTLE (63187-499-30) | 2015-02-02 | | No | Historical |
| 63187-499-60 | 60 TABLET, COATED in 1 BOTTLE (63187-499-60) | 2015-02-02 | | No | Historical |
| 63187-499-90 | 90 TABLET, COATED in 1 BOTTLE (63187-499-90) | 2015-02-02 | | No | Historical |