Package 68788-7665-9
Brand: losartan potassium
Generic: losartan potassiumPackage Facts
Identity
Package NDC
68788-7665-9
Digits Only
6878876659
Product NDC
68788-7665
Description
90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9)
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": "247e9033-04e4-403d-98bd-acbe40d8f987", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["fe1df76d-4925-444d-8e30-9dd07f205fb7"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-7665-1)", "package_ndc": "68788-7665-1", "marketing_start_date": "20200228"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7665-3)", "package_ndc": "68788-7665-3", "marketing_start_date": "20200228"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7665-6)", "package_ndc": "68788-7665-6", "marketing_start_date": "20200228"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7665-9)", "package_ndc": "68788-7665-9", "marketing_start_date": "20200228"}], "brand_name": "Losartan Potassium", "product_id": "68788-7665_247e9033-04e4-403d-98bd-acbe40d8f987", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "68788-7665", "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": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20200228", "listing_expiration_date": "20261231"}