Package 67046-1643-3
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
67046-1643-3
Digits Only
6704616433
Product NDC
67046-1643
Description
30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1643-3)
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": "47ccfb28-5ce1-a24e-e063-6294a90a4207", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["47cd0227-90a5-cdf6-e063-6294a90af661"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1643-3)", "package_ndc": "67046-1643-3", "marketing_start_date": "20260107"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "67046-1643_47ccfb28-5ce1-a24e-e063-6294a90a4207", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1643", "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": "20 mg/1"}], "application_number": "ANDA205519", "marketing_category": "ANDA", "marketing_start_date": "20260107", "listing_expiration_date": "20271231"}