Lisinopril
- Product NDC
- 59115-144
- 11-digit product format
- 591150144
- Labeler code
- 59115
- Product ID
- 59115-144_ecedf718-c763-4bfb-8222-1b9c911587b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hikma Pharmaceutical
- Application
- ANDA076063
- Marketing category
- ANDA
- Marketing start
- 2013-08-22
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record