Quinapril
- Product NDC
- 68001-260
- 11-digit product format
- 680010260
- Labeler code
- 68001
- Product ID
- 68001-260_df08337a-79bd-47c9-858a-8ee32469cfe5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA077690
- Marketing category
- ANDA
- Marketing start
- 2014-07-18
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Quinapril
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| QUINAPRIL HYDROCHLORIDE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 33067B3N2M |
| Rxcui | 312748, 312749, 312750, 314203 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-260-05 | Quinapril | 90 in 1 BOTTLE | TABLET | 90 | | 12 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-260 | QUINAPRIL TABLET [BLUEPOINT LABORATORIES] | 12 | Current NDC, Legacy NDC, 1 package rows | 20200827_1b5809a8-873d-44cb-af59-e0d8fc81b385.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 |
|---|
| 68001-260-05 | 68001026005 | 90 TABLET in 1 BOTTLE (68001-260-05) | 90 tablet | 2014-07-18 | 0000-00-00 | No | No | Current |