Package 72162-1696-0

Brand: losartan potassium tablets, 25 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72162-1696-0
Digits Only 7216216960
Product NDC 72162-1696
Product ID 72162-1696_448a3184-c51b-450f-880c-4eb15084abf7
Description

1000 TABLET in 1 BOTTLE (72162-1696-0)

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand losartan potassium tablets, 25 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Losartan potassium Tablets, 25 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "448a3184-c51b-450f-880c-4eb15084abf7", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["7b8f5329-4fdb-4e1d-98b1-de1ca1b171c5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1696-0)", "package_ndc": "72162-1696-0", "marketing_start_date": "20240206"}], "brand_name": "Losartan potassium Tablets, 25 mg", "product_id": "72162-1696_448a3184-c51b-450f-880c-4eb15084abf7", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72162-1696", "generic_name": "losartan potassium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan potassium Tablets, 25 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA201170", "marketing_category": "ANDA", "marketing_start_date": "20120918", "listing_expiration_date": "20261231"}