Package 82009-178-10
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
82009-178-10
Digits Only
8200917810
Product NDC
82009-178
Description
1000 TABLET, FILM COATED in 1 BOTTLE (82009-178-10)
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": "3cc5dd82-b074-c0e2-e063-6394a90aa46e", "openfda": {"upc": ["0382009176109", "3389449177106"], "unii": ["48A5M73Z4Q"], "rxcui": ["259255", "617310", "617311", "617312"], "spl_set_id": ["5b94b6f4-6f64-4551-abcb-8e845fb13813"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82009-178-10)", "package_ndc": "82009-178-10", "marketing_start_date": "20250801"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "82009-178_3cc5dd82-b074-c0e2-e063-6394a90aa46e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82009-178", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}