Package 70518-4474-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-4474-0
Digits Only 7051844740
Product NDC 70518-4474
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4474-0)

Marketing

Marketing Status
Marketed Since 2025-09-10
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": "3e77a5c6-bb5c-51cf-e063-6294a90a3e4f", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["bd26679f-f8ff-41d2-a384-bd1f66f8a614"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4474-0)", "package_ndc": "70518-4474-0", "marketing_start_date": "20250910"}], "brand_name": "Atorvastatin calcium", "product_id": "70518-4474_3e77a5c6-bb5c-51cf-e063-6294a90a3e4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4474", "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": "40 mg/1"}], "application_number": "ANDA217081", "marketing_category": "ANDA", "marketing_start_date": "20250910", "listing_expiration_date": "20261231"}