zestril

Generic: lisinopril

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zestril
Generic Name lisinopril
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-241
Product ID 24979-241_7875efff-59e3-4f68-84c5-e3c9c16d6a3c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019777
Listing Expiration 2026-12-31
Marketing Start 2024-04-25

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24979241
Hyphenated Format 24979-241

Supplemental Identifiers

RxCUI
104375 104376 104377 104378 197884 205326 206771 213482 311353 311354 314076 314077
UPC
0324979239071 0324979241074 0324979243078 0324979240077 0324979242071 0324979238074
UNII
E7199S1YWR

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zestril (source: ndc)
Generic Name lisinopril (source: ndc)
Application Number NDA019777 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (24979-241-07)
source: ndc

Packages (1)

Ingredients (1)

lisinopril (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7875efff-59e3-4f68-84c5-e3c9c16d6a3c", "openfda": {"upc": ["0324979239071", "0324979241074", "0324979243078", "0324979240077", "0324979242071", "0324979238074"], "unii": ["E7199S1YWR"], "rxcui": ["104375", "104376", "104377", "104378", "197884", "205326", "206771", "213482", "311353", "311354", "314076", "314077"], "spl_set_id": ["838c2d78-d2d8-4981-9ec9-e50ef9e1a5d8"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (24979-241-07)", "package_ndc": "24979-241-07", "marketing_start_date": "20240425"}], "brand_name": "Zestril", "product_id": "24979-241_7875efff-59e3-4f68-84c5-e3c9c16d6a3c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "24979-241", "generic_name": "Lisinopril", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zestril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "NDA019777", "marketing_category": "NDA", "marketing_start_date": "20240425", "listing_expiration_date": "20261231"}