Package 70518-3339-1

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-3339-1
Digits Only 7051833391
Product NDC 70518-3339
Product ID 70518-3339_3a72d52d-68a2-3cd6-e063-6394a90a6354
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3339-1)

Marketing

Marketing Status
Marketed Since 2023-12-19
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": "3a72d52d-68a2-3cd6-e063-6394a90a6354", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["b0bbab86-6789-4ffb-8f84-ee91b69fdb34"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3339-1)", "package_ndc": "70518-3339-1", "marketing_start_date": "20231219"}], "brand_name": "Atorvastatin calcium", "product_id": "70518-3339_3a72d52d-68a2-3cd6-e063-6394a90a6354", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-3339", "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": "20 mg/1"}], "application_number": "ANDA211933", "marketing_category": "ANDA", "marketing_start_date": "20220123", "listing_expiration_date": "20261231"}