lisinopril
- Product NDC
- 68001-272
- 11-digit product format
- 680010272
- Labeler code
- 68001
- Product ID
- 68001-272_9494cf39-52ea-496c-89ac-5915bb2f0d8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA075994
- Marketing category
- ANDA
- Marketing start
- 2016-09-07
- Marketing end
- 2019-08-31
- 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