Package 50090-7529-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 50090-7529-0
Digits Only 5009075290
Product NDC 50090-7529
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7529-0)

Marketing

Marketing Status
Marketed Since 2025-04-07
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5adfc928-9071-4e23-9bb8-1a8506ce4a06", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["9fb1a276-8253-49f0-930e-6e158d643500"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7529-0)", "package_ndc": "50090-7529-0", "marketing_start_date": "20250407"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "50090-7529_5adfc928-9071-4e23-9bb8-1a8506ce4a06", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7529", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20241001", "listing_expiration_date": "20261231"}