Package 50090-7385-0

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 50090-7385-0
Digits Only 5009073850
Product NDC 50090-7385
Product ID 50090-7385_7d542915-3db3-4a51-b52b-f070421cb3fe
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7385-0)

Marketing

Marketing Status
Marketed Since 2024-10-21
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7d542915-3db3-4a51-b52b-f070421cb3fe", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["57b070d1-217a-413b-9350-e2387c5c282a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7385-0)", "package_ndc": "50090-7385-0", "marketing_start_date": "20241021"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "50090-7385_7d542915-3db3-4a51-b52b-f070421cb3fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "50090-7385", "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": "40 mg/1"}], "application_number": "ANDA214344", "marketing_category": "ANDA", "marketing_start_date": "20230912", "listing_expiration_date": "20261231"}