Package 70518-1514-1

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-1514-1
Digits Only 7051815141
Product NDC 70518-1514
Product ID 70518-1514_4913f4a3-a238-7b28-e063-6394a90a2dd7
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1514-1)

Marketing

Marketing Status
Marketed Since 2018-10-19
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": "4913f4a3-a238-7b28-e063-6394a90a2dd7", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["259255"], "spl_set_id": ["7050dd33-a547-4e07-a914-56267ead67ce"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1514-1)", "package_ndc": "70518-1514-1", "marketing_start_date": "20181019"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "70518-1514_4913f4a3-a238-7b28-e063-6394a90a2dd7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-1514", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE", "strength": "80 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20181018", "listing_expiration_date": "20271231"}