Package 51655-756-52

Brand: rosuvastatin calcium

Generic: rosuvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 51655-756-52
Digits Only 5165575652
Product NDC 51655-756
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-756-52)

Marketing

Marketing Status
Marketed Since 2021-07-19
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": "495180de-7ec6-97fa-e063-6294a90adb4d", "openfda": {"unii": ["83MVU38M7Q"], "rxcui": ["859424"], "spl_set_id": ["da6bfffb-7b04-b522-e053-2a95a90a4736"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-756-52)", "package_ndc": "51655-756-52", "marketing_start_date": "20210719"}], "brand_name": "Rosuvastatin Calcium", "product_id": "51655-756_495180de-7ec6-97fa-e063-6294a90adb4d", "dosage_form": "TABLET, COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-756", "generic_name": "Rosuvastatin Calcium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rosuvastatin Calcium", "active_ingredients": [{"name": "ROSUVASTATIN CALCIUM", "strength": "5 mg/1"}], "application_number": "ANDA201619", "marketing_category": "ANDA", "marketing_start_date": "20210719", "listing_expiration_date": "20271231"}