Package 63629-9192-1

Brand: losartan potassium tablets, 50 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 63629-9192-1
Digits Only 6362991921
Product NDC 63629-9192
Product ID 63629-9192_13337021-409e-4c0c-b7ee-3c40b442828d
Description

1000 TABLET in 1 BOTTLE (63629-9192-1)

Marketing

Marketing Status
Marketed Since 2022-08-03
Brand losartan potassium tablets, 50 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan potassium Tablets, 50 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "13337021-409e-4c0c-b7ee-3c40b442828d", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["eea03814-3fb5-4f85-8a4d-18e73057d880"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-9192-1)", "package_ndc": "63629-9192-1", "marketing_start_date": "20220803"}], "brand_name": "Losartan potassium Tablets, 50 mg", "product_id": "63629-9192_13337021-409e-4c0c-b7ee-3c40b442828d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "63629-9192", "generic_name": "losartan potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium Tablets, 50 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA201170", "marketing_category": "ANDA", "marketing_start_date": "20120918", "listing_expiration_date": "20261231"}