Lisinopril
- Product NDC
- 0143-9715
- 11-digit product format
- 001439715
- Labeler code
- 0143
- Product ID
- 0143-9715_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
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0143-9715-01 | 00143971501 | 100 TABLET in 1 BOTTLE (0143-9715-01) | 100 tablet | 2013-02-13 | 0000-00-00 | No | No | Current |
| 0143-9715-10 | 00143971510 | 1000 TABLET in 1 BOTTLE (0143-9715-10) | 1000 tablet | 2013-02-13 | 0000-00-00 | No | No | Current |
| 0143-9715-99 | 00143971599 | 142857 TABLET in 1 DRUM (0143-9715-99) | 142857 tablet | 2013-02-13 | 0000-00-00 | No | No | Current |