Package 50090-6482-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 50090-6482-0
Digits Only 5009064820
Product NDC 50090-6482
Product ID 50090-6482_dbea73a1-6632-4d9f-b87b-4a740a311ce3
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6482-0)

Marketing

Marketing Status
Marketed Since 2023-05-17
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dbea73a1-6632-4d9f-b87b-4a740a311ce3", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617310"], "spl_set_id": ["25015637-c825-487c-ac33-c5ac46a4732f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6482-0)", "package_ndc": "50090-6482-0", "marketing_start_date": "20230517"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "50090-6482_dbea73a1-6632-4d9f-b87b-4a740a311ce3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-6482", "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 PROPYLENE GLYCOL SOLVATE", "strength": "20 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20210801", "listing_expiration_date": "20261231"}