Zestril
- Product NDC
- 24979-241
- 11-digit product format
- 249790241
- Labeler code
- 24979
- Product ID
- 24979-241_7875efff-59e3-4f68-84c5-e3c9c16d6a3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- NDA019777
- Marketing category
- NDA
- Marketing start
- 2024-04-25
- Substance
- LISINOPRIL
- 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
- Zestril
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LISINOPRIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | E7199S1YWR |
| Rxcui | 104375, 104376, 104377, 104378, 197884, 205326, 206771, 213482, 311353, 311354, 314076, 314077 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24979-241-07 | Zestril | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24979-241 | ZESTRIL (LISINOPRIL) TABLET [UPSHER-SMITH LABORATORIES, LLC] | 2 | Current NDC, 1 package rows | 20250503_838c2d78-d2d8-4981-9ec9-e50ef9e1a5d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 24979-241-07 | 24979024107 | 90 TABLET in 1 BOTTLE (24979-241-07) | 90 tablet | 2024-04-25 | No | No | Current |