lisinopril
- Product NDC
- 63187-722
- 11-digit product format
- 631870722
- Labeler code
- 63187
- Product ID
- 63187-722_f2b34441-3099-4719-8436-aad63219b9bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2015-05-23
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63187-722 | LISINOPRIL TABLET [PROFICIENT RX LP] | 3 | Legacy NDC | 20191126_4067b6c7-2a99-4c41-82ec-b47506603c3c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-722-30 | 63187072230 | 30 TABLET in 1 BOTTLE (63187-722-30) | 30 tablet | 2016-06-01 | 0000-00-00 | No | No | Current |
| 63187-722-60 | 63187072260 | 60 TABLET in 1 BOTTLE (63187-722-60) | 60 tablet | 2016-06-01 | 0000-00-00 | No | No | Current |
| 63187-722-90 | 63187072290 | 90 TABLET in 1 BOTTLE (63187-722-90) | 90 tablet | 2016-06-01 | 0000-00-00 | No | No | Current |