Lisinopril
- Product NDC
- 51079-981
- 11-digit product format
- 510790981
- Labeler code
- 51079
- Product ID
- 51079-981_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
- 2019-05-31
- Substance
- LISINOPRIL
- Active strength
- 5 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 |
|---|---|---|---|---|---|
| 51079-981-01 | EA - Each | 51079-981 | 882c1744-7a5f-45e6-b265-ed37f9b65918 | 1 | 2012-07-24 |
| 51079-981-20 | EA - Each | 51079-981 | 26639dce-56e8-48e0-a3cc-0db7909b6155 | 1 | 2012-07-24 |
| 51079-981-30 | EA - Each | 51079-981 | 3648ec6a-16c7-4662-8b4f-c17504dd5973 | 1 | 2012-07-24 |
| 51079-981-40 | EA - Each | 51079-981 | 43041354-3774-44aa-b75a-4d4d4bd596ef | 1 | 2013-02-11 |
| 51079-981-56 | EA - Each | 51079-981 | c4299837-13d7-4f3c-a910-85a418fbf00c | 1 | 2012-07-24 |
| 51079-981-60 | EA - Each | 51079-981 | e644a8f3-f804-4070-bd95-3e6efbb317cb | 1 | 2013-02-11 |