lisinopril

Generic: lisinopril

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lisinopril
Generic Name lisinopril
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lisinopril 40 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7650
Product ID 50090-7650_44726ab1-1e27-4b9b-87dd-14ac91bb6b15
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077321
Listing Expiration 2026-12-31
Marketing Start 2021-06-01

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 500907650
Hyphenated Format 50090-7650

Supplemental Identifiers

RxCUI
197884
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
  • 40 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7650-0)
source: ndc

Packages (1)

50090-7650-0 90 TABLET in 1 BOTTLE (50090-7650-0)

Ingredients (1)

lisinopril (40 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": "44726ab1-1e27-4b9b-87dd-14ac91bb6b15", "openfda": {"unii": ["E7199S1YWR"], "rxcui": ["197884"], "spl_set_id": ["47054448-7d5f-43c4-8313-70179a7f9a2e"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7650-0)", "package_ndc": "50090-7650-0", "marketing_start_date": "20250904"}], "brand_name": "Lisinopril", "product_id": "50090-7650_44726ab1-1e27-4b9b-87dd-14ac91bb6b15", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "50090-7650", "generic_name": "Lisinopril", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril", "active_ingredients": [{"name": "LISINOPRIL", "strength": "40 mg/1"}], "application_number": "ANDA077321", "marketing_category": "ANDA", "marketing_start_date": "20210601", "listing_expiration_date": "20261231"}