Lisinopril
- Product NDC
- 50090-7221
- 11-digit product format
- 500907221
- Labeler code
- 50090
- Product ID
- 50090-7221_1c896ba2-cf3c-4f74-ad6c-d335e2a80316
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- Substance
- LISINOPRIL
- Active strength
- 10 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7221-0 | 50090722100 | 90 TABLET in 1 BOTTLE (50090-7221-0) | 90 tablet | 2024-08-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | A-S Medication Solutions | 2025-10-18 | HUMAN PRESCRIPTION DRUG LABEL | 53 |
| Lisinopril | A-S Medication Solutions | 2024-08-15 | HUMAN PRESCRIPTION DRUG LABEL | 51 |