Lisinopril
- Product NDC
- 0615-8548
- 11-digit product format
- 006158548
- Labeler code
- 0615
- Product ID
- 0615-8548_25cc7469-c2d8-4d68-9286-f4ee8f1ae90f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2017-04-17
- Substance
- LISINOPRIL
- Active strength
- 30 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 |
|---|
| 0615-8548-39 | 00615854839 | 30 TABLET in 1 BLISTER PACK (0615-8548-39) | 30 tablet | 2024-10-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | NCS HealthCare of KY, LLC dba Vangard Labs | 2024-10-18 | HUMAN PRESCRIPTION DRUG LABEL | 18 |