lisinopril
- Product NDC
- 50090-2952
- 11-digit product format
- 500902952
- Labeler code
- 50090
- Product ID
- 50090-2952_7f153589-888a-42c7-92b5-1ac265bc627b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| lisinopril | A-S Medication Solutions | 2018-07-02 | HUMAN PRESCRIPTION DRUG LABEL | 15 |