Lisinopril
- Product NDC
- 51079-983
- 11-digit product format
- 510790983
- Labeler code
- 51079
- Product ID
- 51079-983_7cae77cb-9353-c346-e053-2a91aa0a35c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA076071
- Marketing category
- ANDA
- Marketing start
- 2002-08-01
- Marketing end
- 2019-08-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51079-983-01 | EA - Each | 51079-983 | 0c7875af-484c-462c-b23a-7f86aaedc2e6 | 1 | 2012-07-24 |
| 51079-983-17 | EA - Each | 51079-983 | ec96d674-3923-48d0-b0dd-c7987609c27a | 1 | 2012-07-24 |
| 51079-983-19 | EA - Each | 51079-983 | 1a1a22c4-8b65-4471-aa4c-222b96863d59 | 1 | 2012-07-24 |
| 51079-983-20 | EA - Each | 51079-983 | 4b27334b-8bb0-4525-b2f2-6c7e33ec6db0 | 1 | 2012-07-24 |
| 51079-983-30 | EA - Each | 51079-983 | 8055c18a-0fb9-4c27-bc44-4ebfd66528a4 | 1 | 2012-07-24 |
| 51079-983-40 | EA - Each | 51079-983 | 687eda15-b691-45f9-8d72-50c5678756f3 | 1 | 2013-02-11 |
| 51079-983-56 | EA - Each | 51079-983 | e88e64d5-b7e2-4c48-aff9-4df4a91c3b56 | 1 | 2012-07-24 |
| 51079-983-60 | EA - Each | 51079-983 | 5bb26b64-6526-4aae-9d22-56bc58a240b3 | 1 | 2013-02-11 |