lisinopril

Generic: lisinopril

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler aurobindo pharma limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-038
Product ID 65862-038_02e12641-9edf-4791-8684-5f148f3ed574
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077622
Listing Expiration 2026-12-31
Marketing Start 2006-02-22

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 65862038
Hyphenated Format 65862-038

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0365862038012 0365862040015 0365862037015
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 ANDA077622 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (65862-038-00)
  • 100 TABLET in 1 BOTTLE (65862-038-01)
  • 500 TABLET in 1 BOTTLE (65862-038-05)
  • 30 TABLET in 1 BOTTLE (65862-038-30)
  • 1000 TABLET in 1 BOTTLE (65862-038-99)
source: ndc

Packages (5)

65862-038-00 100 TABLET in 1 BOTTLE (65862-038-00) 65862-038-01 100 TABLET in 1 BOTTLE (65862-038-01) 65862-038-05 500 TABLET in 1 BOTTLE (65862-038-05) 65862-038-30 30 TABLET in 1 BOTTLE (65862-038-30) 65862-038-99 1000 TABLET in 1 BOTTLE (65862-038-99)

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": "02e12641-9edf-4791-8684-5f148f3ed574", "openfda": {"upc": ["0365862038012", "0365862040015", "0365862037015"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["0e6364a4-6d66-4151-8197-d45e2a762895"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-038-00)", "package_ndc": "65862-038-00", "marketing_start_date": "20060222"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-038-01)", "package_ndc": "65862-038-01", "marketing_start_date": "20060222"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-038-05)", "package_ndc": "65862-038-05", "marketing_start_date": "20060222"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-038-30)", "package_ndc": "65862-038-30", "marketing_start_date": "20060222"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-038-99)", "package_ndc": "65862-038-99", "marketing_start_date": "20060222"}], "brand_name": "Lisinopril", "product_id": "65862-038_02e12641-9edf-4791-8684-5f148f3ed574", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "65862-038", "generic_name": "Lisinopril", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "5 mg/1"}], "application_number": "ANDA077622", "marketing_category": "ANDA", "marketing_start_date": "20060222", "listing_expiration_date": "20261231"}