Lisinopril
- Product NDC
- 68788-7831
- 11-digit product format
- 687887831
- Labeler code
- 68788
- Product ID
- 68788-7831_729acd45-cc83-4fa3-b032-66e8e45629c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2021-01-08
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7831-1 | 68788783101 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-7831-1) | 100 tablet | 2021-01-08 | 0000-00-00 | No | No | Current |
| 68788-7831-3 | 68788783103 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-7831-3) | 30 tablet | 2021-01-08 | 0000-00-00 | No | No | Current |
| 68788-7831-6 | 68788783106 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-7831-6) | 60 tablet | 2021-01-08 | 0000-00-00 | No | No | Current |
| 68788-7831-9 | 68788783109 | 90 TABLET in 1 BOTTLE, PLASTIC (68788-7831-9) | 90 tablet | 2021-01-08 | 0000-00-00 | No | No | Current |