lisinopril

Generic: lisinopril

Labeler: solco healthcare u.s., llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler solco healthcare u.s., llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
Solco healthcare U.S., LLC

Identifiers & Regulatory

Product NDC 43547-417
Product ID 43547-417_1ed80b02-cb3b-41c5-ab33-ff0106b8792d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075743
Listing Expiration 2026-12-31
Marketing Start 2017-08-30

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 43547417
Hyphenated Format 43547-417

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0343547414108
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 lisinopril (source: ndc)
Generic Name lisinopril (source: ndc)
Application Number ANDA075743 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 45 TABLET in 1 BOTTLE (43547-417-04)
  • 90 TABLET in 1 BOTTLE (43547-417-09)
  • 100 TABLET in 1 BOTTLE (43547-417-10)
  • 1000 TABLET in 1 BOTTLE (43547-417-11)
  • 5000 TABLET in 1 BOTTLE (43547-417-15)
  • 500 TABLET in 1 BOTTLE (43547-417-50)
source: ndc

Packages (6)

43547-417-04 45 TABLET in 1 BOTTLE (43547-417-04) 43547-417-09 90 TABLET in 1 BOTTLE (43547-417-09) 43547-417-10 100 TABLET in 1 BOTTLE (43547-417-10) 43547-417-11 1000 TABLET in 1 BOTTLE (43547-417-11) 43547-417-15 5000 TABLET in 1 BOTTLE (43547-417-15) 43547-417-50 500 TABLET in 1 BOTTLE (43547-417-50)

Ingredients (1)

lisinopril (20 mg/1)

Linked Drug Pages (1)

Lisinopril ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1ed80b02-cb3b-41c5-ab33-ff0106b8792d", "openfda": {"upc": ["0343547414108"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["f8d16c85-50e2-4d99-afae-6fb902734e42"], "manufacturer_name": ["Solco healthcare U.S., LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET in 1 BOTTLE (43547-417-04)", "package_ndc": "43547-417-04", "marketing_start_date": "20170830"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (43547-417-09)", "package_ndc": "43547-417-09", "marketing_start_date": "20170830"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (43547-417-10)", "package_ndc": "43547-417-10", "marketing_start_date": "20170830"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (43547-417-11)", "package_ndc": "43547-417-11", "marketing_start_date": "20170830"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (43547-417-15)", "package_ndc": "43547-417-15", "marketing_start_date": "20170830"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43547-417-50)", "package_ndc": "43547-417-50", "marketing_start_date": "20170830"}], "brand_name": "Lisinopril", "product_id": "43547-417_1ed80b02-cb3b-41c5-ab33-ff0106b8792d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "43547-417", "generic_name": "Lisinopril", "labeler_name": "Solco healthcare U.S., LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA075743", "marketing_category": "ANDA", "marketing_start_date": "20170830", "listing_expiration_date": "20261231"}