Lisinopril
- Product NDC
- 0143-9713
- 11-digit product format
- 001439713
- Labeler code
- 0143
- Product ID
- 0143-9713_533f6e0f-04a0-4ef7-81b8-0a7be07ddd1a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA076063
- Marketing category
- ANDA
- Marketing start
- 2013-02-13
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
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 |
|---|
| 0143-9713-01 | 00143971301 | 100 TABLET in 1 BOTTLE (0143-9713-01) | 100 tablet | 2013-02-13 | 0000-00-00 | No | No | Current |
| 0143-9713-10 | 00143971310 | 1000 TABLET in 1 BOTTLE (0143-9713-10) | 1000 tablet | 2013-02-13 | 0000-00-00 | No | No | Current |
| 0143-9713-99 | 00143971399 | 68807 TABLET in 1 DRUM (0143-9713-99) | 68807 tablet | 2013-02-13 | 0000-00-00 | No | No | Current |