Benazepril Hydrochloride
- Product NDC
- 68788-7846
- 11-digit product format
- 687887846
- Labeler code
- 68788
- Product ID
- 68788-7846_3244817a-9567-42fb-aab8-5dc1a2fb45fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticlas Inc.
- Application
- ANDA078212
- Marketing category
- ANDA
- Marketing start
- 2021-01-20
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 40 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record