Package 82009-066-10

Brand: lisinopril

Generic: lisinopril
NDC Package

Package Facts

Identity

Package NDC 82009-066-10
Digits Only 8200906610
Product NDC 82009-066
Product ID 82009-066_d2b42923-6e5f-47a1-9b31-4d019142a102
Description

1000 TABLET in 1 BOTTLE (82009-066-10)

Marketing

Marketing Status
Marketed Since 2023-07-07
Brand lisinopril
Generic lisinopril
Sample Package No

Linked Drug Pages (1)

Lisinopril ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d2b42923-6e5f-47a1-9b31-4d019142a102", "openfda": {"upc": ["0382009066103", "0382009062051"], "unii": ["E7199S1YWR"], "rxcui": ["197884", "311353", "311354", "314076", "314077"], "spl_set_id": ["f2e09150-22f2-4028-b214-917d686200ad"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-066-10)", "package_ndc": "82009-066-10", "marketing_start_date": "20230707"}], "brand_name": "Lisinopril", "product_id": "82009-066_d2b42923-6e5f-47a1-9b31-4d019142a102", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]"], "product_ndc": "82009-066", "generic_name": "Lisinopril", "labeler_name": "Quallent Pharmaceuticals Health LLC", "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": "20230707", "listing_expiration_date": "20261231"}