lisinopril
- Product NDC
- 0185-0602
- 11-digit product format
- 001850602
- Labeler code
- 0185
- Product ID
- 0185-0602_a9e1ba16-fb5e-4d16-829c-bada7356fc00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Eon Labs, Inc.
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2015-11-17
- Marketing end
- 2022-05-31
- Substance
- LISINOPRIL
- Active strength
- 3 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0185-0602-01 | 00185060201 | 100 TABLET in 1 BOTTLE (0185-0602-01) | 100 tablet | 2015-11-17 | 2022-04-30 | No | No | Current |
| 0185-0602-10 | 00185060210 | 1000 TABLET in 1 BOTTLE (0185-0602-10) | 1000 tablet | 2015-11-17 | 2022-05-31 | No | No | Current |