Package 72189-100-90
Brand: losartan potassium
Generic: losartan potassiumPackage Facts
Identity
Package NDC
72189-100-90
Digits Only
7218910090
Product NDC
72189-100
Description
90 TABLET, FILM COATED in 1 BOTTLE (72189-100-90)
Marketing
Marketing Status
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": "2be871d4-0d2d-9f90-e063-6294a90ad6d2", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["a58c56b2-e05c-6697-e053-2a95a90ad466"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-100-90)", "package_ndc": "72189-100-90", "marketing_start_date": "20200513"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "72189-100_2be871d4-0d2d-9f90-e063-6294a90ad6d2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-100", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA091497", "marketing_category": "ANDA", "marketing_start_date": "20200513", "listing_expiration_date": "20261231"}