lisinopril
- Product NDC
- 55154-7639
- 11-digit product format
- 551547639
- Labeler code
- 55154
- Product ID
- 55154-7639_dd86594a-a3f6-49e8-86cf-af8a888c5e55
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2015-06-15
- 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 |