Package 68788-8189-6

Brand: losartan potassium

Generic: losartan potassium
NDC Package

Package Facts

Identity

Package NDC 68788-8189-6
Digits Only 6878881896
Product NDC 68788-8189
Description

60 TABLET, FILM COATED in 1 BOTTLE (68788-8189-6)

Marketing

Marketing Status
Marketed Since 2022-05-13
Brand losartan potassium
Generic losartan potassium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "061d0838-f325-4fdb-8eb5-c0684f0df7db", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["68ed9727-987e-4bb6-98b4-b98150bb6404"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8189-1)", "package_ndc": "68788-8189-1", "marketing_start_date": "20220513"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8189-3)", "package_ndc": "68788-8189-3", "marketing_start_date": "20220513"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8189-6)", "package_ndc": "68788-8189-6", "marketing_start_date": "20220513"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8189-9)", "package_ndc": "68788-8189-9", "marketing_start_date": "20220513"}], "brand_name": "Losartan Potassium", "product_id": "68788-8189_061d0838-f325-4fdb-8eb5-c0684f0df7db", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-8189", "generic_name": "Losartan potassium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20220513", "listing_expiration_date": "20261231"}