Package 70518-4550-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-4550-0
Digits Only 7051845500
Product NDC 70518-4550
Product ID 70518-4550_48d20cf1-5a59-d787-e063-6294a90ac997
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4550-0)

Marketing

Marketing Status
Marketed Since 2026-01-19
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": "48d20cf1-5a59-d787-e063-6294a90ac997", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["f15094eb-3161-441e-b8ea-c33db2af6b50"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4550-0)", "package_ndc": "70518-4550-0", "marketing_start_date": "20260119"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "70518-4550_48d20cf1-5a59-d787-e063-6294a90ac997", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4550", "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": "10 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20260119", "listing_expiration_date": "20271231"}