LISINOPRIL
- Product NDC
- 50436-0352
- 11-digit product format
- 504360352
- Labeler code
- 50436
- Product ID
- 50436-0352_c4d985d0-4007-4f6a-87d4-60f8a00254c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA076180
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 50436-0352-1 | LISINOPRIL | 30 in 1 BOTTLE | TABLET | 30 | | 18 |
| 50436-0352-3 | LISINOPRIL | 90 in 1 BOTTLE | TABLET | 90 | | 18 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0352 | LISINOPRIL TABLET [UNIT DOSE SERVICES] | 18 | Legacy NDC, 2 package rows | 20230110_e65f2d8c-a4f6-40ba-a85d-8ee7806bd65f.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 |
|---|
| 50436-0352-1 | 50436035201 | 30 TABLET in 1 BOTTLE (50436-0352-1) | 30 tablet | 2017-08-04 | 0000-00-00 | No | No | Current |
| 50436-0352-3 | 50436035203 | 90 TABLET in 1 BOTTLE (50436-0352-3) | 90 tablet | 2017-08-04 | 0000-00-00 | No | No | Current |