Package 72162-1698-0

Brand: losartan potassium tablets, 100 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72162-1698-0
Digits Only 7216216980
Product NDC 72162-1698
Product ID 72162-1698_479a9534-5c54-4a49-8656-08897c62a73d
Description

1000 TABLET in 1 BOTTLE (72162-1698-0)

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand losartan potassium tablets, 100 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan potassium Tablets, 100 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "479a9534-5c54-4a49-8656-08897c62a73d", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["726002cf-2d95-4dac-b1f6-e7f92bb13496"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1698-0)", "package_ndc": "72162-1698-0", "marketing_start_date": "20240206"}], "brand_name": "Losartan potassium Tablets, 100 mg", "product_id": "72162-1698_479a9534-5c54-4a49-8656-08897c62a73d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72162-1698", "generic_name": "losartan potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium Tablets, 100 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA201170", "marketing_category": "ANDA", "marketing_start_date": "20120918", "listing_expiration_date": "20261231"}