Lisinopril
- Product NDC
- 60760-390
- 11-digit product format
- 607600390
- Labeler code
- 60760
- Product ID
- 60760-390_a00e3e70-9122-aebe-e053-2995a90a68ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2020-03-02
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| E7199S1YWR | LISINOPRIL | 83915-83-7 | LISINOPRIL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-390-90 | 60760039090 | 90 TABLET in 1 BOTTLE, PLASTIC (60760-390-90) | 90 tablet | 2020-03-02 | 0000-00-00 | No | No | Current |