Package 72189-065-90

Brand: rosuvastatin

Generic: rosuvastatin
NDC Package

Package Facts

Identity

Package NDC 72189-065-90
Digits Only 7218906590
Product NDC 72189-065
Description

90 TABLET, FILM COATED in 1 BOTTLE (72189-065-90)

Marketing

Marketing Status
Marketed Since 2019-12-10
Brand rosuvastatin
Generic rosuvastatin
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c499576-6f7a-6e58-e063-6294a90ab6a0", "openfda": {"unii": ["83MVU38M7Q"], "rxcui": ["859419", "859424"], "spl_set_id": ["99602058-4681-7cb5-e053-2995a90a099c"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-065-30)", "package_ndc": "72189-065-30", "marketing_start_date": "20191210"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-065-90)", "package_ndc": "72189-065-90", "marketing_start_date": "20191210"}], "brand_name": "ROSUVASTATIN", "product_id": "72189-065_4c499576-6f7a-6e58-e063-6294a90ab6a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72189-065", "generic_name": "ROSUVASTATIN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ROSUVASTATIN", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "5 mg/1"}], "application_number": "ANDA208898", "marketing_category": "ANDA", "marketing_start_date": "20191210", "listing_expiration_date": "20271231"}