Package 72189-096-30
Brand: losartan potassium
Generic: losartan potassiumPackage Facts
Identity
Package NDC
72189-096-30
Digits Only
7218909630
Product NDC
72189-096
Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-096-30)
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": "2be86a22-266a-f811-e063-6294a90acb38", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["a5b5da65-a4d5-1bd5-e053-2a95a90a6a60"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-096-30)", "package_ndc": "72189-096-30", "marketing_start_date": "20200515"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-096-90)", "package_ndc": "72189-096-90", "marketing_start_date": "20200515"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "72189-096_2be86a22-266a-f811-e063-6294a90acb38", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-096", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20200515", "listing_expiration_date": "20261231"}