Package 70518-1322-1

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-1322-1
Digits Only 7051813221
Product NDC 70518-1322
Product ID 70518-1322_48d6a1d8-b643-2332-e063-6294a90af0ab
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1322-1)

Marketing

Marketing Status
Marketed Since 2018-07-25
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": "48d6a1d8-b643-2332-e063-6294a90af0ab", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617311"], "spl_set_id": ["303989c9-823e-4bcb-a7b3-7024fd0d3a38"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1322-1)", "package_ndc": "70518-1322-1", "marketing_start_date": "20180725"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "70518-1322_48d6a1d8-b643-2332-e063-6294a90af0ab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-1322", "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": "40 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20180725", "listing_expiration_date": "20271231"}