Benazepril Hydrochloride
- Product NDC
- 55154-5672
- 11-digit product format
- 551545672
- Labeler code
- 55154
- Product ID
- 55154-5672_1e279593-b095-4836-b65b-acbdef1742e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- benazepril hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076430
- Marketing category
- ANDA
- Marketing start
- 2004-05-21
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 20 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record