lisinopril

Generic: lisinopril

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 30 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 82868-009
Product ID 82868-009_4833b1b2-c5b1-7dd1-e063-6294a90a7f6b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2027-12-31
Marketing Start 2023-08-21

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 82868009
Hyphenated Format 82868-009

Supplemental Identifiers

RxCUI
205326
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
  • 30 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (82868-009-30)
source: ndc

Packages (1)

82868-009-30 30 TABLET in 1 BOTTLE, PLASTIC (82868-009-30)

Ingredients (1)

lisinopril (30 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": "4833b1b2-c5b1-7dd1-e063-6294a90a7f6b", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["205326"], "spl_set_id": ["03fe066f-c3d7-fa71-e063-6294a90ac6f6"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-009-30)", "package_ndc": "82868-009-30", "marketing_start_date": "20230821"}], "brand_name": "Lisinopril", "product_id": "82868-009_4833b1b2-c5b1-7dd1-e063-6294a90a7f6b", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "82868-009", "generic_name": "Lisinopril", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "30 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20230821", "listing_expiration_date": "20271231"}