Package 51655-256-52
Brand: rosuvastatin calcium
Generic: rosuvastatin calciumPackage Facts
Identity
Package NDC
51655-256-52
Digits Only
5165525652
Product NDC
51655-256
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-256-52)
Marketing
Marketing Status
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": "48e6b7ae-bba7-5b4d-e063-6394a90a2d61", "openfda": {"unii": ["83MVU38M7Q"], "rxcui": ["859747"], "spl_set_id": ["f80b8d59-2c22-8fff-e053-6294a90a2f9e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-256-52)", "package_ndc": "51655-256-52", "marketing_start_date": "20230322"}], "brand_name": "Rosuvastatin calcium", "product_id": "51655-256_48e6b7ae-bba7-5b4d-e063-6394a90a2d61", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "51655-256", "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": "10 mg/1"}], "application_number": "ANDA079172", "marketing_category": "ANDA", "marketing_start_date": "20230322", "listing_expiration_date": "20271231"}