Quinapril
- Product NDC
- 50090-4649
- 11-digit product format
- 500904649
- Labeler code
- 50090
- Product ID
- 50090-4649_43b3534d-dee0-4175-8ea3-b385a810adaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078457
- Marketing category
- ANDA
- Marketing start
- 2016-07-22
- Marketing end
- 0000-00-00
- Substance
- QUINAPRIL HYDROCHLORIDE
- Active strength
- 40 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-4649-0 | Quinapril | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
| 50090-4649-1 | Quinapril | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-4649 | QUINAPRIL TABLET [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 2 package rows | 20210417_9225ff95-2886-4429-ac91-f20147ffae94.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4649-0 | 50090464900 | 30 TABLET in 1 BOTTLE (50090-4649-0) | 30 tablet | 2019-10-25 | 0000-00-00 | No | No | Current |
| 50090-4649-1 | 50090464901 | 90 TABLET in 1 BOTTLE (50090-4649-1) | 90 tablet | 2019-10-25 | 0000-00-00 | No | No | Current |