Package 63629-8471-1

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 63629-8471-1
Digits Only 6362984711
Product NDC 63629-8471
Description

90 TABLET, FILM COATED in 1 BOTTLE (63629-8471-1)

Marketing

Marketing Status
Marketed Since 2016-05-19
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": "4ff3852d-482e-4ce1-a3a2-a2f019f40fc8", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["635addf1-2024-4675-8d3c-380dc4548fbd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-8471-1)", "package_ndc": "63629-8471-1", "marketing_start_date": "20160519"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "63629-8471_4ff3852d-482e-4ce1-a3a2-a2f019f40fc8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "63629-8471", "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"}