LISINOPRIL
- Product NDC
- 50090-2934
- 11-digit product format
- 500902934
- Labeler code
- 50090
- Product ID
- 50090-2934_edb45974-3b4a-42e7-ba48-ddfa488b1e25
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076164
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Substance
- LISINOPRIL
- Active strength
- 30 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 50090-2934-0 | 50090293400 | 30 TABLET in 1 BOTTLE (50090-2934-0) | 30 tablet | 2017-03-27 | No | No | Historical |
| 50090-2934-1 | 50090293401 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-2934-1) | 90 tablet | 2014-11-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LISINOPRIL | A-S Medication Solutions | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL | 27 |