lisinopril

Generic: lisinopril

Labeler: legacy pharmaceutical packaging, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler legacy pharmaceutical packaging, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-532
Product ID 68645-532_4742db84-1ab9-25f5-e063-6394a90a1859
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2017-03-07

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 68645532
Hyphenated Format 68645-532

Supplemental Identifiers

RxCUI
314077
UPC
0368645532547
UNII
E7199S1YWR

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 ANDA077321 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68645-532-54)
source: ndc

Packages (1)

68645-532-54 30 TABLET in 1 BOTTLE (68645-532-54)

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": "4742db84-1ab9-25f5-e063-6394a90a1859", "openfda": {"upc": ["0368645532547"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["2688aa37-1ab9-4353-8689-8c2347ec5d3c"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68645-532-54)", "package_ndc": "68645-532-54", "marketing_start_date": "20170307"}], "brand_name": "Lisinopril", "product_id": "68645-532_4742db84-1ab9-25f5-e063-6394a90a1859", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68645-532", "generic_name": "Lisinopril", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20170307", "listing_expiration_date": "20261231"}