Lisinopril
- Product NDC
- 50090-4678
- 11-digit product format
- 500904678
- Labeler code
- 50090
- Product ID
- 50090-4678_fa9ae3ea-c77e-4cc0-b2fa-8f751dbe6cd4
- 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
- 3 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 50090-4678-0 | 50090467800 | 30 TABLET in 1 BOTTLE (50090-4678-0) | 30 tablet | 2019-11-04 | 0000-00-00 | No | No | Current |
| 50090-4678-1 | 50090467801 | 100 TABLET in 1 BOTTLE, PLASTIC (50090-4678-1) | 100 tablet | 2019-11-04 | 0000-00-00 | No | No | Current |
| 50090-4678-2 | 50090467802 | 90 TABLET in 1 BOTTLE (50090-4678-2) | 90 tablet | 2019-11-04 | 0000-00-00 | No | No | Current |