Lisinopril
- Product NDC
- 71610-406
- 11-digit product format
- 716100406
- Labeler code
- 71610
- Product ID
- 71610-406_75ff1aad-8d47-4263-9c2e-29fe43b720e4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA075743
- Marketing category
- ANDA
- Marketing start
- 2017-08-30
- Substance
- LISINOPRIL
- Active strength
- 40 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 |
|---|
| 71610-406-60 | 71610040660 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-406-60) | 90 tablet | 2020-03-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | Aphena Pharma Solutions - Tennessee, LLC | 2020-04-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |