Lisinopril
- Product NDC
- 68788-9750
- 11-digit product format
- 687889750
- Labeler code
- 68788
- Product ID
- 68788-9750_118c25b7-6e2f-45dd-b760-342dab6a3526
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA076063
- Marketing category
- ANDA
- Marketing start
- 2012-01-30
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record