Lisinopril
- Product NDC
- 50090-7022
- 11-digit product format
- 500907022
- Labeler code
- 50090
- Product ID
- 50090-7022_676bbf3b-2b1e-40b2-98c0-a2333e84aef9
- 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 |
|---|
| 50090-7022-0 | 50090702200 | 100 BLISTER PACK in 1 CARTON (50090-7022-0) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2024-01-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | A-S Medication Solutions | 2024-01-09 | HUMAN PRESCRIPTION DRUG LABEL | 51 |