Package 42291-906-90

Brand: pitavastatin

Generic: pitavastatin calcium
NDC Package

Package Facts

Identity

Package NDC 42291-906-90
Digits Only 4229190690
Product NDC 42291-906
Description

90 TABLET, FILM COATED in 1 BOTTLE (42291-906-90)

Marketing

Marketing Status
Marketed Since 2024-01-16
Brand pitavastatin
Generic pitavastatin calcium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48843604-c6e9-1aec-e063-6294a90aea80", "openfda": {"unii": ["IYD54XEG3W"], "rxcui": ["861643", "861648", "861652"], "spl_set_id": ["0f11ee80-871e-4f13-e063-6394a90af19d"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42291-906-90)", "package_ndc": "42291-906-90", "marketing_start_date": "20240116"}], "brand_name": "Pitavastatin", "product_id": "42291-906_48843604-c6e9-1aec-e063-6294a90aea80", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42291-906", "generic_name": "pitavastatin calcium", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pitavastatin", "active_ingredients": [{"name": "PITAVASTATIN CALCIUM", "strength": "2.09 mg/1"}], "application_number": "ANDA205932", "marketing_category": "ANDA", "marketing_start_date": "20240116", "listing_expiration_date": "20271231"}