Package 70518-3946-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-3946-0
Digits Only 7051839460
Product NDC 70518-3946
Description

30 TABLET in 1 BLISTER PACK (70518-3946-0)

Marketing

Marketing Status
Discontinued 2026-04-01
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": "287445ec-d6a0-1932-e063-6294a90af0bc", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["5369137c-28a0-400c-8502-36dc066f528f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3946-0)", "package_ndc": "70518-3946-0", "marketing_end_date": "20260401", "marketing_start_date": "20231209"}], "brand_name": "atorvastatin calcium", "product_id": "70518-3946_287445ec-d6a0-1932-e063-6294a90af0bc", "dosage_form": "TABLET", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-3946", "generic_name": "atorvastatin calcium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA206536", "marketing_category": "ANDA", "marketing_end_date": "20260401", "marketing_start_date": "20231209"}