LISINOPRIL
- Product NDC
- 71610-612
- 11-digit product format
- 716100612
- Labeler code
- 71610
- Product ID
- 71610-612_7fce9fa4-5381-42ba-a267-46c75292c59a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076180
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- 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 |
|---|
| 71610-612-45 | 71610061245 | 45 TABLET in 1 BOTTLE (71610-612-45) | 45 tablet | 2022-01-31 | No | No | Historical |
| 71610-612-60 | 71610061260 | 90 TABLET in 1 BOTTLE (71610-612-60) | 90 tablet | 2021-11-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LISINOPRIL | Aphena Pharma Solutions - Tennessee, LLC | 2022-02-22 | HUMAN PRESCRIPTION DRUG LABEL | 2 |