Package 70518-0186-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-0186-0
Digits Only 7051801860
Product NDC 70518-0186
Product ID 70518-0186_47e48249-8eb4-26a5-e063-6394a90a4330
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0186-0)

Marketing

Marketing Status
Marketed Since 2017-01-31
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47e48249-8eb4-26a5-e063-6394a90a4330", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617310"], "spl_set_id": ["e91c673d-c26c-4ff1-90d2-2b9d47a8d771"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0186-0)", "package_ndc": "70518-0186-0", "marketing_start_date": "20170131"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "70518-0186_47e48249-8eb4-26a5-e063-6394a90a4330", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-0186", "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": "20 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20170131", "listing_expiration_date": "20271231"}