Lisinopril
- Product NDC
- 0904-7200
- 11-digit product format
- 009047200
- Labeler code
- 0904
- Product ID
- 0904-7200_5efe4f9d-62f8-4c2e-a8ef-37c1a1ca0b3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2021-06-01
- Substance
- LISINOPRIL
- Active strength
- 40 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 |
|---|
| 0904-7200-61 | 00904720061 | 100 BLISTER PACK in 1 CARTON (0904-7200-61) / 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2021-06-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Lisinopril | Major Pharmaceuticals | 2025-07-18 | HUMAN PRESCRIPTION DRUG LABEL | 6 |