Lisinopril
- Product NDC
- 50090-2989
- 11-digit product format
- 500902989
- Labeler code
- 50090
- Product ID
- 50090-2989_2650ef9f-5ed7-4fae-9d3d-4f6844206247
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2017-05-12
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2989 | LISINOPRIL TABLET LISINOPRIL TABLET [A-S MEDICATION SOLUTIONS] | 59 | Legacy NDC, 5 package rows | 20250406_34953f77-bae1-41fe-af11-3ea0b3ceaa11.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2989-0 | 50090298900 | 30 TABLET in 1 BOTTLE (50090-2989-0) | 30 tablet | 2017-05-12 | 0000-00-00 | No | No | Current |
| 50090-2989-1 | 50090298901 | 100 in 1 BOTTLE | | | | | | Historical |
| 50090-2989-3 | 50090298903 | 60 TABLET in 1 BOTTLE (50090-2989-3) | 60 tablet | 2017-05-12 | 0000-00-00 | No | No | Current |
| 50090-2989-4 | 50090298904 | 200 TABLET in 1 BOTTLE (50090-2989-4) | 200 tablet | 2017-05-12 | 0000-00-00 | No | No | Current |
| 50090-2989-5 | 50090298905 | 90 TABLET in 1 BOTTLE (50090-2989-5) | 90 tablet | 2017-05-12 | 0000-00-00 | No | No | Current |