LISINOPRIL
- Product NDC
- 61919-942
- 11-digit product format
- 619190942
- Labeler code
- 61919
- Product ID
- 61919-942_9c97a803-9d98-691e-e053-2995a90ab7c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISINOPRIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2017-02-20
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-942-90 | LISINOPRIL | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-942 | LISINOPRIL TABLET [DIRECT RX] | 2 | Legacy NDC, 1 package rows | 20200121_48f813f1-700f-3d8f-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-942-90 | 61919094290 | 90 TABLET in 1 BOTTLE (61919-942-90) | 90 tablet | 2017-02-20 | 0000-00-00 | No | No | Current |