lisinopril
- Product NDC
- 70882-110
- 11-digit product format
- 708820110
- Labeler code
- 70882
- Product ID
- 70882-110_84eceb98-cd51-4392-b808-371bb0bc420d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cambridge Therapeutics Technologies, LLC
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2015-05-23
- 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
- 2020-12-31
- 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 |
|---|
| 70882-110-30 | lisinopril | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70882-110 | LISINOPRIL TABLET LISINOPRIL TABLET [CAMBRIDGE THERAPEUTICS TECHNOLOGIES, LLC] | 2 | Legacy NDC, 1 package rows | 20170227_585f3757-7978-4887-bda9-d072be286482.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 |
|---|
| 70882-110-30 | 70882011030 | 30 TABLET in 1 BLISTER PACK (70882-110-30) | 30 tablet | 2015-05-23 | 0000-00-00 | No | No | Current |