Package 67046-1453-3

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 67046-1453-3
Digits Only 6704614533
Product NDC 67046-1453
Product ID 67046-1453_2d93e13a-a441-d1c5-e063-6394a90aee3f
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1453-3)

Marketing

Marketing Status
Marketed Since 2025-02-07
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (1)

ATORVASTATIN CALCIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d93e13a-a441-d1c5-e063-6394a90aee3f", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["2d93e3c4-59cc-cff4-e063-6394a90a8f7f"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1453-3)", "package_ndc": "67046-1453-3", "marketing_start_date": "20250207"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "67046-1453_2d93e13a-a441-d1c5-e063-6394a90aee3f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1453", "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": "ANDA205945", "marketing_category": "ANDA", "marketing_start_date": "20250207", "listing_expiration_date": "20261231"}