Quinapril
- Product NDC
- 71335-1441
- 11-digit product format
- 713351441
- Labeler code
- 71335
- Product ID
- 71335-1441_4d680b89-d236-4f15-9d29-d3f584093e3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2014-08-01
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1441-1 | 71335144101 | 30 TABLET in 1 BOTTLE (71335-1441-1) | 30 tablet | 2019-12-19 | 0000-00-00 | No | No | Current |
| 71335-1441-2 | 71335144102 | 60 TABLET in 1 BOTTLE (71335-1441-2) | 60 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1441-3 | 71335144103 | 90 TABLET in 1 BOTTLE (71335-1441-3) | 90 tablet | 2019-12-17 | 0000-00-00 | No | No | Current |
| 71335-1441-4 | 71335144104 | 180 TABLET in 1 BOTTLE (71335-1441-4) | 180 tablet | 2020-03-11 | 0000-00-00 | No | No | Current |