Quinapril
- Product NDC
- 62135-486
- 11-digit product format
- 621350486
- Labeler code
- 62135
- Product ID
- 62135-486_09cd5cb9-4fdf-f133-e063-6294a90af691
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Quinapril
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA076803
- Marketing category
- ANDA
- Marketing start
- 2005-03-02
- 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
- 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 | 20 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 |
|---|
| 62135-486-90 | Quinapril | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-486 | QUINAPRIL TABLET, FILM COATED [CHARTWELL RX, LLC] | 1 | Current NDC, 1 package rows | 20231111_dbc43dbd-94aa-40e2-a9ea-766110cc8687.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-486-90 | 62135048690 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-486-90) | 2023-11-06 | No | No | Historical |