Lisinopril
- Product NDC
- 50090-4485
- 11-digit product format
- 500904485
- Labeler code
- 50090
- Product ID
- 50090-4485_7f85a561-a628-4561-a7f5-fa5ff96a8ffc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4485-0 | 50090448500 | 33 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-4485-0) > 1 TABLET in 1 BLISTER PACK | 33 blister pack | 2019-08-29 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | A-S Medication Solutions | 2019-09-06 | HUMAN PRESCRIPTION DRUG LABEL | 2 |