LISINOPRIL
- Product NDC
- 71335-0176
- 11-digit product format
- 713350176
- Labeler code
- 71335
- Product ID
- 71335-0176_86139e2b-1a97-4fa6-8bba-1ee01cae1281
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076164
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Substance
- LISINOPRIL
- Active strength
- 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 |
|---|
| 71335-0176-1 | 71335017601 | 30 TABLET in 1 BOTTLE (71335-0176-1) | 30 tablet | 2018-02-27 | No | No | Historical |
| 71335-0176-2 | 71335017602 | 90 TABLET in 1 BOTTLE (71335-0176-2) | 90 tablet | 2018-03-16 | No | No | Historical |
| 71335-0176-3 | 71335017603 | 60 TABLET in 1 BOTTLE (71335-0176-3) | 60 tablet | 2022-10-12 | No | No | Historical |
| 71335-0176-4 | 71335017604 | 100 TABLET in 1 BOTTLE (71335-0176-4) | 100 tablet | 2018-03-28 | No | No | Historical |
| 71335-0176-5 | 71335017605 | 10 TABLET in 1 BOTTLE (71335-0176-5) | 10 tablet | 2019-03-19 | No | No | Historical |
| 71335-0176-6 | 71335017606 | 28 TABLET in 1 BOTTLE (71335-0176-6) | 28 tablet | 2024-10-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LISINOPRIL | Bryant Ranch Prepack | 2024-10-08 | HUMAN PRESCRIPTION DRUG LABEL | 102 |