LISINOPRIL
- Product NDC
- 68071-5046
- 11-digit product format
- 680715046
- Labeler code
- 68071
- Product ID
- 68071-5046_1b415bf6-3e3c-92d7-e063-6394a90a39a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076180
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Substance
- LISINOPRIL
- Active strength
- 2.5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 68071-5046-1 | 68071504601 | 100 TABLET in 1 BOTTLE (68071-5046-1) | 100 tablet | 2019-08-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LISINOPRIL | NuCare Pharmaceuticals,Inc. | 2024-06-19 | HUMAN PRESCRIPTION DRUG LABEL | 3 |