Package 82009-042-10

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 82009-042-10
Digits Only 8200904210
Product NDC 82009-042
Product ID 82009-042_55d92567-c635-4877-91cb-dd142c71c4fb
Description

1000 TABLET, FILM COATED in 1 BOTTLE (82009-042-10)

Marketing

Marketing Status
Marketed Since 2022-09-20
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan Potassium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "55d92567-c635-4877-91cb-dd142c71c4fb", "openfda": {"upc": ["0382009044101"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["1a9e1ffd-edf1-4e35-a7f5-ca351c507d7f"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82009-042-10)", "package_ndc": "82009-042-10", "marketing_start_date": "20220920"}], "brand_name": "Losartan Potassium", "product_id": "82009-042_55d92567-c635-4877-91cb-dd142c71c4fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "82009-042", "generic_name": "Losartan Potassium", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA078243", "marketing_category": "ANDA", "marketing_start_date": "20220920", "listing_expiration_date": "20271231"}