Quinapril
- Product NDC
- 68084-899
- 11-digit product format
- 680840899
- Labeler code
- 68084
- Product ID
- 68084-899_ea3fb07f-0005-8a55-e053-2a95a90a8243
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2015-09-24
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 20 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 |
|---|
| 68084-899-25 | 68084089925 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-899-25) > 1 TABLET in 1 BLISTER PACK (68084-899-95) | 30 blister pack | 2015-09-24 | 0000-00-00 | No | No | Current |