Package 67046-1491-3

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 67046-1491-3
Digits Only 6704614913
Product NDC 67046-1491
Product ID 67046-1491_2cd99334-31e3-10ef-e063-6294a90acc1e
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1491-3)

Marketing

Marketing Status
Marketed Since 2025-01-29
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": "2cd99334-31e3-10ef-e063-6294a90acc1e", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["2cd9999b-e18f-09de-e063-6294a90a108b"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1491-3)", "package_ndc": "67046-1491-3", "marketing_start_date": "20250129"}], "brand_name": "Atorvastatin calcium", "product_id": "67046-1491_2cd99334-31e3-10ef-e063-6294a90acc1e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "67046-1491", "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": "ANDA217081", "marketing_category": "ANDA", "marketing_start_date": "20250129", "listing_expiration_date": "20261231"}