Quinapril
- Product NDC
- 68788-6894
- 11-digit product format
- 687886894
- Labeler code
- 68788
- Product ID
- 68788-6894_f22c564b-8d47-416c-a0a2-f7de83deb26a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202725
- Marketing category
- ANDA
- Marketing start
- 2017-02-13
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-6894-1 | 68788689401 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-6894-1) | 2017-02-13 | 0000-00-00 | No | No | Current |
| 68788-6894-3 | 68788689403 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-6894-3) | 2017-02-13 | 0000-00-00 | No | No | Current |
| 68788-6894-6 | 68788689406 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-6894-6) | 2017-02-13 | 0000-00-00 | No | No | Current |
| 68788-6894-9 | 68788689409 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-6894-9) | 2017-02-13 | 0000-00-00 | No | No | Current |