lisinopril

Generic: lisinopril

Labeler: xlcare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler xlcare pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 10 mg/1

Manufacturer
XLCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 72865-210
Product ID 72865-210_c008ecb6-970d-4ac9-9402-e21e8d9d76b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075903
Listing Expiration 2026-12-31
Marketing Start 2021-08-17

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 72865210
Hyphenated Format 72865-210

Supplemental Identifiers

RxCUI
197884 205326 311353 311354 314076 314077
UPC
0372865210505 0372865212059 0372865211502 0372865213100
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 ANDA075903 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72865-210-01)
  • 1000 TABLET in 1 BOTTLE (72865-210-10)
  • 45 TABLET in 1 BOTTLE (72865-210-45)
  • 5000 TABLET in 1 BOTTLE (72865-210-50)
  • 90 TABLET in 1 BOTTLE (72865-210-90)
source: ndc

Packages (5)

72865-210-01 100 TABLET in 1 BOTTLE (72865-210-01) 72865-210-10 1000 TABLET in 1 BOTTLE (72865-210-10) 72865-210-45 45 TABLET in 1 BOTTLE (72865-210-45) 72865-210-50 5000 TABLET in 1 BOTTLE (72865-210-50) 72865-210-90 90 TABLET in 1 BOTTLE (72865-210-90)

Ingredients (1)

lisinopril (10 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": "c008ecb6-970d-4ac9-9402-e21e8d9d76b2", "openfda": {"upc": ["0372865210505", "0372865212059", "0372865211502", "0372865213100"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "205326", "311353", "311354", "314076", "314077"], "spl_set_id": ["c008ecb6-970d-4ac9-9402-e21e8d9d76b2"], "manufacturer_name": ["XLCare Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-210-01)", "package_ndc": "72865-210-01", "marketing_start_date": "20210817"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72865-210-10)", "package_ndc": "72865-210-10", "marketing_start_date": "20210817"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (72865-210-45)", "package_ndc": "72865-210-45", "marketing_start_date": "20210817"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (72865-210-50)", "package_ndc": "72865-210-50", "marketing_start_date": "20210817"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72865-210-90)", "package_ndc": "72865-210-90", "marketing_start_date": "20210817"}], "brand_name": "Lisinopril", "product_id": "72865-210_c008ecb6-970d-4ac9-9402-e21e8d9d76b2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "72865-210", "generic_name": "Lisinopril", "labeler_name": "XLCare Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA075903", "marketing_category": "ANDA", "marketing_start_date": "20210817", "listing_expiration_date": "20261231"}