Package 67046-1505-3

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 67046-1505-3
Digits Only 6704615053
Product NDC 67046-1505
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1505-3)

Marketing

Marketing Status
Marketed Since 2025-01-25
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": "2c93e2aa-de18-0fec-e063-6394a90aa541", "openfda": {"upc": ["0370756248125"], "unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["2c67a15c-53b7-f431-e063-6394a90acc50"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1505-3)", "package_ndc": "67046-1505-3", "marketing_start_date": "20250125"}], "brand_name": "Atorvastatin calcium", "product_id": "67046-1505_2c93e2aa-de18-0fec-e063-6394a90aa541", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1505", "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": "ANDA217081", "marketing_category": "ANDA", "marketing_start_date": "20250125", "listing_expiration_date": "20261231"}