Lisinopril
- Product NDC
- 63629-8823
- 11-digit product format
- 636298823
- Labeler code
- 63629
- Product ID
- 63629-8823_188a507d-0741-406d-bee9-a75e344eecdb
- 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 |
|---|
| 63629-8823-1 | 63629882301 | 100 TABLET in 1 BOTTLE, PLASTIC (63629-8823-1) | 100 tablet | 2021-09-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | Bryant Ranch Prepack | 2024-01-15 | HUMAN PRESCRIPTION DRUG LABEL | 102 |