LISINOPRIL
- Product NDC
- 35356-879
- 11-digit product format
- 353560879
- Labeler code
- 35356
- Product ID
- 35356-879_54f3bc99-fd78-4501-a6d4-5e151cddb504
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LISINOPRIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2007-02-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 35356-879-30 | 35356087930 | 30 TABLET in 1 BOTTLE (35356-879-30) | 30 tablet | 2013-09-16 | 0000-00-00 | No | No | Current |