Lisinopril
- Product NDC
- 0591-0407
- 11-digit product format
- 005910407
- Labeler code
- 0591
- Product ID
- 0591-0407_01764c1d-aebe-4a46-920c-4b5f8cca8acb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA076059
- Marketing category
- ANDA
- Marketing start
- 2002-07-01
- 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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Lisinopril
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LISINOPRIL | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | E7199S1YWR |
| Rxcui | 197884, 205326, 311353, 311354, 314076, 314077 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0591-0407-01 | Lisinopril | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 35 |
| 0591-0407-10 | Lisinopril | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 35 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| LISINOPRIL | ACTIVE INGREDIENT | E7199S1YWR | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| LISINOPRIL ANHYDROUS | ACTIVE MOIETY | 7Q3P4BS2FD | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| ALUMINUM OXIDE | INACTIVE INGREDIENT | LMI26O6933 | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE | INACTIVE INGREDIENT | O7TSZ97GEP | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| FD&C BLUE NO. 2 | INACTIVE INGREDIENT | L06K8R7DQK | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| FD&C YELLOW NO. 5 | INACTIVE INGREDIENT | I753WB2F1M | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | LISINOPRIL TABLET [WATSON LABORATORIES, INC.] | 20 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0591-0407 | LISINOPRIL TABLET [ACTAVIS PHARMA, INC.] | 35 | Current NDC, Legacy NDC, 2 package rows | 20230913_43e2c8d1-3704-4323-bcaf-f582572b81f7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-0407-00 | 00591040700 | 50000 TABLET in 1 BOX (0591-0407-00) | 50000 tablet | 01-JUL-02 | | | | Current |
| 0591-0407-01 | 00591040701 | 100 TABLET in 1 BOTTLE, PLASTIC (0591-0407-01) | 100 tablet | 2002-07-01 | 0000-00-00 | No | No | Current |
| 0591-0407-10 | 00591040710 | 1000 TABLET in 1 BOTTLE, PLASTIC (0591-0407-10) | 1000 tablet | 2002-07-01 | 0000-00-00 | No | No | Current |