LISINOPRIL
- Product NDC
- 61919-356
- 11-digit product format
- 619190356
- Labeler code
- 61919
- Product ID
- 61919-356_76f5f437-1d95-4073-a4bd-23e4cbb3b9ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISINOPRIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DirectRX
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 61919-356-30 | LISINOPRIL | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-356 | LISINOPRIL TABLET [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151023_02d8b170-72a9-4987-91d8-d655e6aaf2cd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 61919-356-30 | 61919035630 | 30 in 1 BOTTLE | Historical |