Package 50268-709-15

Brand: rosuvastatin

Generic: rosuvastatin
NDC Package

Package Facts

Identity

Package NDC 50268-709-15
Digits Only 5026870915
Product NDC 50268-709
Description

50 BLISTER PACK in 1 BOX (50268-709-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-709-11)

Marketing

Marketing Status
Marketed Since 2018-12-14
Brand rosuvastatin
Generic rosuvastatin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39ff0f38-7c7a-4ce1-e063-6394a90aa663", "openfda": {"unii": ["83MVU38M7Q"], "rxcui": ["859419", "859747", "859751"], "spl_set_id": ["7cd6ae8d-aa67-60db-e053-2991aa0a0ede"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-709-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-709-11)", "package_ndc": "50268-709-15", "marketing_start_date": "20181214"}], "brand_name": "Rosuvastatin", "product_id": "50268-709_39ff0f38-7c7a-4ce1-e063-6394a90aa663", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50268-709", "generic_name": "Rosuvastatin", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "10 mg/1"}], "application_number": "ANDA207616", "marketing_category": "ANDA", "marketing_start_date": "20181214", "listing_expiration_date": "20261231"}