Lisinopril
- Product NDC
- 0603-4212
- 11-digit product format
- 006034212
- Labeler code
- 0603
- Product ID
- 0603-4212_434b11ef-3ccb-4284-ba8b-14ceea66e030
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Par Pharmaceutical
- Application
- ANDA075743
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 2019-04-30
- 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 Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f8f05a6d-f74b-4e9e-ab1c-374d3b4fb820 | Product name | 1 | 20230703 |
| f65307a7-3644-0a09-cdfd-94aae8d3b53e | Product name | 3 | 20210902 |
| 1bdb87cf-9b1f-6a51-5eb7-d182aaffaa3d | Product name | 2 | 20170719 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0603-4212-02 | EA - Each | 0603-4212 | 1690be2c-4cf6-4a84-9c49-bef52075e620 | 1 | 2012-07-24 |
| 0603-4212-21 | EA - Each | 0603-4212 | 7bdfd2a9-30d9-464b-954c-f791a0c28cbe | 1 | 2012-07-24 |
| 0603-4212-28 | EA - Each | 0603-4212 | 2537b329-5952-4d03-82b9-5b9e0f22747c | 1 | 2012-07-24 |
| 0603-4212-32 | EA - Each | 0603-4212 | 3a3e7916-9087-496d-9fa9-f49f76dda9fe | 1 | 2012-07-24 |
| 0603-4212-34 | EA - Each | 0603-4212 | ceb683c7-bba3-4cb1-8174-9a51f85f5d48 | 1 | 2012-07-24 |
| 0603-4212-60 | EA - Each | 0603-4212 | ed25967d-249b-404a-a0d9-92ebd93b2c62 | 1 | 2012-07-24 |