Lisinopril
- Product NDC
- 68180-516
- 11-digit product format
- 681800516
- Labeler code
- 68180
- Product ID
- 68180-516_6723a96d-02f8-40c2-95ec-89a7053a7117
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lisinopril
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA077321
- Marketing category
- ANDA
- Marketing start
- 2006-01-13
- Substance
- LISINOPRIL
- Active strength
- 30 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 | 30 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | E7199S1YWR |
| Rxcui | 197884, 205326, 311353, 311354, 314076, 314077 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-516 | LISINOPRIL TABLET [LUPIN PHARMACEUTICALS, INC.] | 21 | Current NDC, Legacy NDC, 5 package rows | 20240308_7d6c31e2-b5a4-4279-8013-a8dad37ea73b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68180-516-01 | 68180051601 | 100 in 1 BOTTLE | Historical |
| 68180-516-02 | 68180051602 | 500 in 1 BOTTLE | Historical |
| 68180-516-03 | 68180051603 | 1000 in 1 BOTTLE | Historical |
| 68180-516-09 | 68180051609 | 90 in 1 BOTTLE | Historical |
| 68180-516-30 | 68180051630 | 5000 in 1 POUCH | Historical |