Package 70518-4199-0

Brand: rosuvastatin calcium

Generic: rosuvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 70518-4199-0
Digits Only 7051841990
Product NDC 70518-4199
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4199-0)

Marketing

Marketing Status
Marketed Since 2024-10-01
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": "3ff4de68-921a-a01d-e063-6294a90a3caf", "openfda": {"unii": ["83MVU38M7Q"], "rxcui": ["859751"], "spl_set_id": ["c607da3c-47f5-4773-8391-2a7b0826d30e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4199-0)", "package_ndc": "70518-4199-0", "marketing_start_date": "20241001"}], "brand_name": "Rosuvastatin calcium", "product_id": "70518-4199_3ff4de68-921a-a01d-e063-6294a90a3caf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "70518-4199", "generic_name": "Rosuvastatin calcium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin calcium", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "20 mg/1"}], "application_number": "ANDA079172", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}