Package 82804-234-30

Brand: rosuvastatin calcium

Generic: rosuvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 82804-234-30
Digits Only 8280423430
Product NDC 82804-234
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-234-30)

Marketing

Marketing Status
Marketed Since 2025-08-13
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": "45033c5f-4246-491a-8707-10f840ff2b6c", "openfda": {"upc": ["0382804234301"], "unii": ["83MVU38M7Q"], "rxcui": ["859424"], "spl_set_id": ["45033c5f-4246-491a-8707-10f840ff2b6c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-234-30)", "package_ndc": "82804-234-30", "marketing_start_date": "20250813"}], "brand_name": "Rosuvastatin calcium", "product_id": "82804-234_45033c5f-4246-491a-8707-10f840ff2b6c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82804-234", "generic_name": "Rosuvastatin calcium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin calcium", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "5 mg/1"}], "application_number": "ANDA079172", "marketing_category": "ANDA", "marketing_start_date": "20160719", "listing_expiration_date": "20261231"}