Package 50090-6714-0
Brand: losartan potassium
Generic: losartan potassiumPackage Facts
Identity
Package NDC
50090-6714-0
Digits Only
5009067140
Product NDC
50090-6714
Description
90 TABLET, FILM COATED in 1 BOTTLE (50090-6714-0)
Marketing
Marketing Status
Brand
losartan potassium
Generic
losartan potassium
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39775c40-a0bd-4981-be4e-0ea1cfa7c321", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979485"], "spl_set_id": ["cff0c9eb-fafd-48e7-a053-036b676bf57d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6714-0)", "package_ndc": "50090-6714-0", "marketing_start_date": "20231004"}], "brand_name": "Losartan Potassium", "product_id": "50090-6714_39775c40-a0bd-4981-be4e-0ea1cfa7c321", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-6714", "generic_name": "Losartan Potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "25 mg/1"}], "application_number": "ANDA090083", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}