Package 68071-3267-9
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
68071-3267-9
Digits Only
6807132679
Product NDC
68071-3267
Description
90 TABLET, FILM COATED in 1 BOTTLE (68071-3267-9)
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": "2d53fdee-0fc2-2c7f-e063-6294a90ab8f2", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["51f23212-a10d-4cfa-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3267-9)", "package_ndc": "68071-3267-9", "marketing_start_date": "20170614"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "68071-3267_2d53fdee-0fc2-2c7f-e063-6294a90ab8f2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68071-3267", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA205519", "marketing_category": "ANDA", "marketing_start_date": "20160804", "listing_expiration_date": "20261231"}