Lisinopril
- Product NDC
- 71205-626
- 11-digit product format
- 712050626
- Labeler code
- 71205
- Product ID
- 71205-626_55a57d80-6bed-44a3-b3ea-6bb44c34cbfc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- Substance
- LISINOPRIL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71205-626-30 | 71205062630 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-626-30) | 30 tablet | 2021-12-14 | No | No | Historical |
| 71205-626-60 | 71205062660 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-626-60) | 60 tablet | 2021-12-14 | No | No | Historical |
| 71205-626-90 | 71205062690 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-626-90) | 90 tablet | 2021-12-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | Proficient Rx LP | 2021-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |