lisinopril

Generic: lisinopril

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-180
Product ID 71205-180_08f51d35-49e2-4f93-8298-c54065cf021c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2017-03-07

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 71205180
Hyphenated Format 71205-180

Supplemental Identifiers

RxCUI
314077
UPC
0371205180003
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
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71205-180-00)
  • 30 TABLET in 1 BOTTLE (71205-180-30)
  • 60 TABLET in 1 BOTTLE (71205-180-60)
  • 90 TABLET in 1 BOTTLE (71205-180-90)
source: ndc

Packages (4)

71205-180-00 100 TABLET in 1 BOTTLE (71205-180-00) 71205-180-30 30 TABLET in 1 BOTTLE (71205-180-30) 71205-180-60 60 TABLET in 1 BOTTLE (71205-180-60) 71205-180-90 90 TABLET in 1 BOTTLE (71205-180-90)

Ingredients (1)

lisinopril (20 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": "08f51d35-49e2-4f93-8298-c54065cf021c", "openfda": {"upc": ["0371205180003"], "unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["b2d493bf-f4d8-4941-8c54-2728d769f6ed"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71205-180-00)", "package_ndc": "71205-180-00", "marketing_start_date": "20200821"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-180-30)", "package_ndc": "71205-180-30", "marketing_start_date": "20181201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-180-60)", "package_ndc": "71205-180-60", "marketing_start_date": "20181201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-180-90)", "package_ndc": "71205-180-90", "marketing_start_date": "20181201"}], "brand_name": "Lisinopril", "product_id": "71205-180_08f51d35-49e2-4f93-8298-c54065cf021c", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "71205-180", "generic_name": "Lisinopril", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20170307", "listing_expiration_date": "20261231"}