Zestril
- Product NDC
- 70518-1451
- 11-digit product format
- 705181451
- Labeler code
- 70518
- Product ID
- 70518-1451_92ded40f-0252-d5f5-e053-2995a90ae7fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA019777
- Marketing category
- NDA
- Marketing start
- 2018-10-02
- Marketing end
- 0000-00-00
- Substance
- LISINOPRIL
- Active strength
- 10 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