Package 67046-1442-3
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
67046-1442-3
Digits Only
6704614423
Product NDC
67046-1442
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1442-3)
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": "2de6c979-6b84-5bea-e063-6394a90a3713", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["2de6b9b3-8f3c-599e-e063-6394a90aee60"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1442-3)", "package_ndc": "67046-1442-3", "marketing_start_date": "20250211"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "67046-1442_2de6c979-6b84-5bea-e063-6394a90a3713", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1442", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20250211", "listing_expiration_date": "20261231"}