QUINAPRIL
- Product NDC
- 70934-964
- 11-digit product format
- 709340964
- Labeler code
- 70934
- Product ID
- 70934-964_dda96c21-bdbf-1c98-e053-2995a90a24f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA205823
- Marketing category
- ANDA
- Marketing start
- 2022-04-27
- 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 |
|---|
| 70934-964-30 | 70934096430 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-964-30) | 30 tablet | 2022-04-27 | 0000-00-00 | No | No | Current |