Quinapril
- Product NDC
- 55154-1032
- 11-digit product format
- 551541032
- Labeler code
- 55154
- Product ID
- 55154-1032_8c54b68f-cc5b-4e97-9253-b9c2c439da59
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA078457
- Marketing category
- ANDA
- Marketing start
- 2012-01-20
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record