Quinapril
- Product NDC
- 50090-5165
- 11-digit product format
- 500905165
- Labeler code
- 50090
- Product ID
- 50090-5165_1e34bba6-cf5f-4400-8c85-c7b396d1e3ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2007-02-26
- 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
- 2022-12-31
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5165-0 | 50090516500 | 30 TABLET in 1 BOTTLE (50090-5165-0) | 30 tablet | 2020-09-23 | 0000-00-00 | No | No | Current |
| 50090-5165-1 | 50090516501 | 90 TABLET in 1 BOTTLE (50090-5165-1) | 90 tablet | 2020-09-23 | 0000-00-00 | No | No | Current |