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 40 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-335
Product ID 51655-335_48eb0bba-4c41-73b4-e063-6294a90a7a83
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076164
Listing Expiration 2027-12-31
Marketing Start 2020-05-21

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 51655335
Hyphenated Format 51655-335

Supplemental Identifiers

RxCUI
197884
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
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-335-26)
source: ndc

Packages (1)

51655-335-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-335-26)

Ingredients (1)

lisinopril (40 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": "48eb0bba-4c41-73b4-e063-6294a90a7a83", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884"], "spl_set_id": ["ab2f8ab5-3c87-484a-e053-2995a90a42bb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-335-26)", "package_ndc": "51655-335-26", "marketing_start_date": "20200521"}], "brand_name": "LISINOPRIL", "product_id": "51655-335_48eb0bba-4c41-73b4-e063-6294a90a7a83", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "51655-335", "generic_name": "Lisinopril", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL", "active_ingredients": [{"name": "LISINOPRIL", "strength": "40 mg/1"}], "application_number": "ANDA076164", "marketing_category": "ANDA", "marketing_start_date": "20200521", "listing_expiration_date": "20271231"}