Package 72789-179-90

Brand: losartan potassium 50 mg

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 72789-179-90
Digits Only 7278917990
Product NDC 72789-179
Product ID 72789-179_4af906c5-4409-7659-e063-6394a90a49ee
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-179-90)

Marketing

Marketing Status
Marketed Since 2021-03-24
Brand losartan potassium 50 mg
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

LOSARTAN POTASSIUM 50 mg ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4af906c5-4409-7659-e063-6394a90a49ee", "openfda": {"upc": ["0372789179902"], "unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["498f26a1-5030-4f9b-9599-07d50e912d41"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-179-90)", "package_ndc": "72789-179-90", "marketing_start_date": "20210324"}], "brand_name": "LOSARTAN POTASSIUM 50 mg", "product_id": "72789-179_4af906c5-4409-7659-e063-6394a90a49ee", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72789-179", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "brand_name_suffix": "50 mg", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA090382", "marketing_category": "ANDA", "marketing_start_date": "20191009", "listing_expiration_date": "20271231"}