Package 70518-0224-1

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-0224-1
Digits Only 7051802241
Product NDC 70518-0224
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0224-1)

Marketing

Marketing Status
Marketed Since 2017-02-16
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": "47e560c6-bd20-1264-e063-6394a90a0048", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617312"], "spl_set_id": ["d57720ab-9f83-4da9-a57f-0d55e00a605c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0224-1)", "package_ndc": "70518-0224-1", "marketing_start_date": "20170216"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "70518-0224_47e560c6-bd20-1264-e063-6394a90a0048", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-0224", "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": "10 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20170215", "listing_expiration_date": "20271231"}