Package 75834-257-25
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
75834-257-25
Digits Only
7583425725
Product NDC
75834-257
Description
2500 TABLET in 1 BOTTLE (75834-257-25)
Marketing
Marketing Status
Brand
atorvastatin calcium
Generic
atorvastatin calcium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4580fe3c-b524-3a14-e063-6294a90a34d3", "openfda": {"nui": ["N0000175589", "N0000000121"], "upc": ["0375834258027", "0375834257501", "0375834255903", "0375834256016"], "unii": ["A0JWA85V8F"], "rxcui": ["259255", "617310", "617311", "617312"], "spl_set_id": ["7c58bf4a-4a92-4db8-89bc-4de1b5831efc"], "pharm_class_epc": ["HMG-CoA Reductase Inhibitor [EPC]"], "pharm_class_moa": ["Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "manufacturer_name": ["NIVAGEN PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (75834-257-01)", "package_ndc": "75834-257-01", "marketing_start_date": "20200826"}, {"sample": false, "description": "2500 TABLET in 1 BOTTLE (75834-257-25)", "package_ndc": "75834-257-25", "marketing_start_date": "20200826"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (75834-257-50)", "package_ndc": "75834-257-50", "marketing_start_date": "20200826"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (75834-257-90)", "package_ndc": "75834-257-90", "marketing_start_date": "20200826"}], "brand_name": "Atorvastatin calcium", "product_id": "75834-257_4580fe3c-b524-3a14-e063-6294a90a34d3", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "75834-257", "generic_name": "Atorvastatin calcium", "labeler_name": "NIVAGEN PHARMACEUTICALS, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN", "strength": "40 mg/1"}], "application_number": "ANDA213853", "marketing_category": "ANDA", "marketing_start_date": "20200826", "listing_expiration_date": "20261231"}