Package 63629-8470-1
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
63629-8470-1
Digits Only
6362984701
Product NDC
63629-8470
Description
500 TABLET, FILM COATED in 1 BOTTLE (63629-8470-1)
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": "b65734de-9d94-4930-9657-b7c7a3c6a2a5", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["66df5c0b-be89-4fc7-8f8d-c7689952c662"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-8470-1)", "package_ndc": "63629-8470-1", "marketing_start_date": "20160519"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "63629-8470_b65734de-9d94-4930-9657-b7c7a3c6a2a5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "63629-8470", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA205519", "marketing_category": "ANDA", "marketing_start_date": "20160519", "listing_expiration_date": "20261231"}