Package 72603-480-01

Brand: pitavastatin calcium

Generic: pitavastatin calcium
NDC Package

Package Facts

Identity

Package NDC 72603-480-01
Digits Only 7260348001
Product NDC 72603-480
Description

90 TABLET, FILM COATED in 1 BOTTLE (72603-480-01)

Marketing

Marketing Status
Marketed Since 2024-12-01
Brand pitavastatin calcium
Generic pitavastatin calcium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27e1ba97-23bf-fc12-e063-6394a90a1699", "openfda": {"unii": ["IYD54XEG3W"], "rxcui": ["861648", "861652"], "spl_set_id": ["98e3f1df-5b38-4169-a340-adb145eac459"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72603-480-01)", "package_ndc": "72603-480-01", "marketing_start_date": "20241201"}], "brand_name": "pitavastatin calcium", "product_id": "72603-480_27e1ba97-23bf-fc12-e063-6394a90a1699", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72603-480", "generic_name": "pitavastatin calcium", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "pitavastatin calcium", "active_ingredients": [{"name": "PITAVASTATIN CALCIUM", "strength": "4.18 mg/1"}], "application_number": "ANDA205977", "marketing_category": "ANDA", "marketing_start_date": "20241201", "listing_expiration_date": "20261231"}