Quinapril
- Product NDC
- 70934-602
- 11-digit product format
- 709340602
- Labeler code
- 70934
- Product ID
- 70934-602_ab848c99-c926-13d7-e053-2a95a90a53fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA202725
- Marketing category
- ANDA
- Marketing start
- 2020-03-05
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-602-30 | 70934060230 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-602-30) | 2020-03-05 | 0000-00-00 | No | No | Current |