Lisinopril
- Product NDC
- 70518-0402
- 11-digit product format
- 705180402
- Labeler code
- 70518
- Product ID
- 70518-0402_848c6f7d-96a1-7a50-e053-2991aa0a89bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076071
- Marketing category
- ANDA
- Marketing start
- 2017-04-05
- 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