Lisinopril
- Product NDC
- 64679-928
- 11-digit product format
- 646790928
- Labeler code
- 64679
- Product ID
- 64679-928_b760b89e-02b4-8439-e053-2a95a90a9de6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Wockhardt USA LLC.
- Application
- ANDA078402
- Marketing category
- ANDA
- Marketing start
- 2007-04-19
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64679-928 | LISINOPRIL TABLET [WOCKHARDT USA LLC.] | 5 | Legacy NDC | 20201227_e927801e-5de4-44f9-b543-789c093de655.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64679-928-01 | 64679092801 | 100 TABLET in 1 BOTTLE (64679-928-01) | 100 tablet | 2007-04-19 | 0000-00-00 | No | No | Current |
| 64679-928-02 | 64679092802 | 3000 TABLET in 1 BOTTLE (64679-928-02) | 3000 tablet | 2007-04-19 | 0000-00-00 | No | No | Current |
| 64679-928-03 | 64679092803 | 10 BLISTER PACK in 1 CARTON (64679-928-03) > 10 TABLET in 1 BLISTER PACK | 10 blister pack | 2007-04-19 | 0000-00-00 | No | No | Current |
| 64679-928-05 | 64679092805 | 500 TABLET in 1 BOTTLE (64679-928-05) | 500 tablet | 2007-04-19 | 0000-00-00 | No | No | Current |
| 64679-928-06 | 64679092806 | 1000 TABLET in 1 BOTTLE (64679-928-06) | 1000 tablet | 2007-04-19 | 0000-00-00 | No | No | Current |