Lisinopril
- Product NDC
- 63629-8079
- 11-digit product format
- 636298079
- Labeler code
- 63629
- Product ID
- 63629-8079_b84e2360-15e6-4555-8d5d-c24d53f58b7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 63629-8079-1 | 63629807901 | 90 TABLET in 1 BOTTLE (63629-8079-1) | 90 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |
| 63629-8079-2 | 63629807902 | 30 TABLET in 1 BOTTLE (63629-8079-2) | 30 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |