Lisinopril
- Product NDC
- 51079-982
- 11-digit product format
- 510790982
- Labeler code
- 51079
- Product ID
- 51079-982_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
- 10 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 |
|---|---|---|---|---|---|
| 51079-982-01 | EA - Each | 51079-982 | 24d9e39f-6033-4db3-90c7-fb850910d790 | 1 | 2012-07-24 |
| 51079-982-17 | EA - Each | 51079-982 | e29f97fa-5fd3-426e-bb87-1434673aed11 | 1 | 2012-07-24 |
| 51079-982-19 | EA - Each | 51079-982 | 4a98ffb6-26b3-481d-bfc4-85a464d9e85d | 1 | 2012-07-24 |
| 51079-982-20 | EA - Each | 51079-982 | 9ab149bf-e2e1-4c8b-8502-b0dc18bd6f7a | 1 | 2012-07-24 |
| 51079-982-30 | EA - Each | 51079-982 | 225ca902-5959-4bf5-ba48-81f76c93ae15 | 1 | 2012-07-24 |
| 51079-982-40 | EA - Each | 51079-982 | 930b3e9c-5345-421c-ac56-d98cf10ce881 | 1 | 2013-02-11 |
| 51079-982-56 | EA - Each | 51079-982 | 3e52c806-a2ab-4528-875f-bd67f35c6381 | 1 | 2012-07-24 |
| 51079-982-60 | EA - Each | 51079-982 | ef1db029-f0a0-47d8-9007-1f99618285ac | 1 | 2013-02-11 |