Quinapril
- Product NDC
- 71335-1707
- 11-digit product format
- 713351707
- Labeler code
- 71335
- Product ID
- 71335-1707_ac824409-47c6-4f5c-b68a-87cb2806af8c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2007-02-26
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 33067B3N2M | QUINAPRIL HYDROCHLORIDE | 82586-55-8 | QUINAPRIL HYDROCHLORIDE |
| RJ84Y44811 | QUINAPRIL | 85441-61-8 | Quinapril |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-1707-1 | 71335170701 | 30 TABLET in 1 BOTTLE (71335-1707-1) | 30 tablet | 2020-09-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Quinapril Tablets USP | Bryant Ranch Prepack | 2024-05-20 | HUMAN PRESCRIPTION DRUG LABEL | 103 |