lisinopril

Generic: lisinopril

Labeler: qpharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler qpharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 20 mg/1

Manufacturer
QPharma, Inc.

Identifiers & Regulatory

Product NDC 42708-165
Product ID 42708-165_4681a929-3969-1024-e063-6394a90a0935
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2017-05-12

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 42708165
Hyphenated Format 42708-165

Supplemental Identifiers

RxCUI
314077
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
  • 30 TABLET in 1 BOTTLE, PLASTIC (42708-165-30)
source: ndc

Packages (1)

42708-165-30 30 TABLET in 1 BOTTLE, PLASTIC (42708-165-30)

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": "4681a929-3969-1024-e063-6394a90a0935", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["f6f68322-f8a1-9011-e053-6394a90a1d2c"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE, PLASTIC (42708-165-30)", "package_ndc": "42708-165-30", "marketing_start_date": "20230315"}], "brand_name": "Lisinopril", "product_id": "42708-165_4681a929-3969-1024-e063-6394a90a0935", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "42708-165", "generic_name": "Lisinopril", "labeler_name": "QPharma, Inc.", "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": "20170512", "listing_expiration_date": "20261231"}