Lisinopril
- Product NDC
- 63629-8736
- 11-digit product format
- 636298736
- Labeler code
- 63629
- Product ID
- 63629-8736_dfbbb798-0f35-42fd-b9f5-d3a7b69a4e3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Substance
- LISINOPRIL
- Active strength
- 2.5 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 |
|---|
| 63629-8736-1 | 63629873601 | 500 TABLET in 1 BOTTLE, PLASTIC (63629-8736-1) | 500 tablet | 2021-08-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | Bryant Ranch Prepack | 2024-01-11 | HUMAN PRESCRIPTION DRUG LABEL | 102 |