Package 70518-4143-2

Brand: rosuvastatin calcium

Generic: rosuvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-4143-2
Digits Only 7051841432
Product NDC 70518-4143
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4143-2)

Marketing

Marketing Status
Marketed Since 2024-07-29
Brand rosuvastatin calcium
Generic rosuvastatin calcium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4cab8619-71f3-7e8e-e063-6294a90a52b0", "openfda": {"unii": ["83MVU38M7Q"], "spl_set_id": ["94245f53-2892-4209-8c94-c32c87d5b106"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4143-2)", "package_ndc": "70518-4143-2", "marketing_start_date": "20240729"}], "brand_name": "Rosuvastatin calcium", "product_id": "70518-4143_4cab8619-71f3-7e8e-e063-6294a90a52b0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4143", "generic_name": "Rosuvastatin calcium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin calcium", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "10 mg/1"}], "application_number": "ANDA079172", "marketing_category": "ANDA", "marketing_start_date": "20240717", "listing_expiration_date": "20271231"}