Benazepril Hydrochloride
- Product NDC
- 68788-9946
- 11-digit product format
- 687889946
- Labeler code
- 68788
- Product ID
- 68788-9946_c76d5a81-cdc3-4de7-a3aa-b2f5525f48a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA076402
- Marketing category
- ANDA
- Marketing start
- 2012-01-12
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record