lisinopril
- Product NDC
- 10544-904
- 11-digit product format
- 105440904
- Labeler code
- 10544
- Product ID
- 10544-904_132542d2-a736-2043-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2015-02-19
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| lisinopril | Blenheim Pharmacal, Inc. | 2015-04-07 | HUMAN PRESCRIPTION DRUG LABEL | 3 |