lisinopril

Generic: lisinopril

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0176
Product ID 71335-0176_86139e2b-1a97-4fa6-8bba-1ee01cae1281
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076164
Listing Expiration 2026-12-31
Marketing Start 2011-11-01

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 713350176
Hyphenated Format 71335-0176

Supplemental Identifiers

RxCUI
311354
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 ANDA076164 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0176-1)
  • 90 TABLET in 1 BOTTLE (71335-0176-2)
  • 60 TABLET in 1 BOTTLE (71335-0176-3)
  • 100 TABLET in 1 BOTTLE (71335-0176-4)
  • 10 TABLET in 1 BOTTLE (71335-0176-5)
  • 28 TABLET in 1 BOTTLE (71335-0176-6)
source: ndc

Packages (6)

71335-0176-1 30 TABLET in 1 BOTTLE (71335-0176-1) 71335-0176-2 90 TABLET in 1 BOTTLE (71335-0176-2) 71335-0176-3 60 TABLET in 1 BOTTLE (71335-0176-3) 71335-0176-4 100 TABLET in 1 BOTTLE (71335-0176-4) 71335-0176-5 10 TABLET in 1 BOTTLE (71335-0176-5) 71335-0176-6 28 TABLET in 1 BOTTLE (71335-0176-6)

Ingredients (1)

lisinopril (5 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": "86139e2b-1a97-4fa6-8bba-1ee01cae1281", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["311354"], "spl_set_id": ["0bf433cb-bf7d-4b41-9518-400646f9aa2a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0176-1)", "package_ndc": "71335-0176-1", "marketing_start_date": "20180227"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0176-2)", "package_ndc": "71335-0176-2", "marketing_start_date": "20180316"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0176-3)", "package_ndc": "71335-0176-3", "marketing_start_date": "20221012"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0176-4)", "package_ndc": "71335-0176-4", "marketing_start_date": "20180328"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-0176-5)", "package_ndc": "71335-0176-5", "marketing_start_date": "20190319"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0176-6)", "package_ndc": "71335-0176-6", "marketing_start_date": "20241008"}], "brand_name": "LISINOPRIL", "product_id": "71335-0176_86139e2b-1a97-4fa6-8bba-1ee01cae1281", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71335-0176", "generic_name": "Lisinopril", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}