LISINOPRIL
- Product NDC
- 70518-0845
- 11-digit product format
- 705180845
- Labeler code
- 70518
- Product ID
- 70518-0845_4845821f-fc64-be02-e063-6394a90aeb42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076164
- Marketing category
- ANDA
- Marketing start
- 2017-11-13
- Substance
- LISINOPRIL
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LISINOPRIL
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LISINOPRIL | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | E7199S1YWR |
| Rxcui | 314077 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-0845-0 | LISINOPRIL | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 6 |
| 70518-0845-1 | LISINOPRIL | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 6 |
| 70518-0845-2 | LISINOPRIL | 30 in 1 BLISTER PACK | TABLET | 30 | | 6 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-0845-0 | 70518084500 | 30 in 1 BOTTLE, PLASTIC | | | | | Historical |
| 70518-0845-1 | 70518084501 | 100 in 1 BOTTLE, PLASTIC | | | | | Historical |
| 70518-0845-2 | 70518084502 | 30 TABLET in 1 BLISTER PACK (70518-0845-2) | 30 tablet | 2025-10-29 | No | No | Historical |