Lisinopril
- Product NDC
- 55154-8128
- 11-digit product format
- 551548128
- Labeler code
- 55154
- Product ID
- 55154-8128_6dd13c87-baea-4e5c-8ec8-1dddd271d14e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- Active strength
- 20 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 |
|---|
| 55154-8128-0 | 55154812800 | 1 BLISTER PACK in 1 BAG (55154-8128-0) > 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2002-07-01 | 0000-00-00 | No | No | Current |