Lisinopril
- Product NDC
- 42708-095
- 11-digit product format
- 427080095
- Labeler code
- 42708
- Product ID
- 42708-095_9f05cf28-0e05-4e86-a495-4af18f52352d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA075743
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#