Lisinopril
- Product NDC
- 0615-8064
- 11-digit product format
- 006158064
- Labeler code
- 0615
- Product ID
- 0615-8064_4643015f-3f68-4ecd-909f-85e3fd2c8549
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076164
- Marketing category
- ANDA
- Marketing start
- 2011-11-01
- Marketing end
- 2020-10-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record