lisinopril

Generic: lisinopril

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

Drug Facts

Product Profile

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

lisinopril 20 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-8351
Product ID 68788-8351_85b2cd38-732d-4047-ac69-5374f28a7cd2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2023-02-07

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 687888351
Hyphenated Format 68788-8351

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
  • 100 TABLET in 1 BOTTLE (68788-8351-1)
  • 30 TABLET in 1 BOTTLE (68788-8351-3)
  • 60 TABLET in 1 BOTTLE (68788-8351-6)
  • 90 TABLET in 1 BOTTLE (68788-8351-9)
source: ndc

Packages (4)

68788-8351-1 100 TABLET in 1 BOTTLE (68788-8351-1) 68788-8351-3 30 TABLET in 1 BOTTLE (68788-8351-3) 68788-8351-6 60 TABLET in 1 BOTTLE (68788-8351-6) 68788-8351-9 90 TABLET in 1 BOTTLE (68788-8351-9)

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": "85b2cd38-732d-4047-ac69-5374f28a7cd2", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["314077"], "spl_set_id": ["b53aee22-52c7-47b1-95fc-e5383b5e6f58"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8351-1)", "package_ndc": "68788-8351-1", "marketing_start_date": "20230207"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8351-3)", "package_ndc": "68788-8351-3", "marketing_start_date": "20230207"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8351-6)", "package_ndc": "68788-8351-6", "marketing_start_date": "20230207"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8351-9)", "package_ndc": "68788-8351-9", "marketing_start_date": "20230207"}], "brand_name": "Lisinopril", "product_id": "68788-8351_85b2cd38-732d-4047-ac69-5374f28a7cd2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "68788-8351", "generic_name": "Lisinopril", "labeler_name": "Preferred Pharmaceuticals, 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": "20230207", "listing_expiration_date": "20261231"}