Zestril
- Product NDC
- 70518-1741
- 11-digit product format
- 705181741
- Labeler code
- 70518
- Product ID
- 70518-1741_967d5a0b-f2fb-3e59-e053-2a95a90a61f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA019777
- Marketing category
- NDA
- Marketing start
- 2018-12-18
- 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