LISINOPRIL
- Product NDC
- 71610-588
- 11-digit product format
- 716100588
- Labeler code
- 71610
- Product ID
- 71610-588_2f083ab0-ee16-4094-97f2-534bf35296d6
- 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
- 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 |
|---|
| 71610-588-60 | 71610058860 | 90 TABLET in 1 BOTTLE (71610-588-60) | 90 tablet | 2021-08-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LISINOPRIL | Aphena Pharma Solutions - Tennessee, LLC | 2021-08-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |