Package 82009-002-10

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 82009-002-10
Digits Only 8200900210
Product NDC 82009-002
Product ID 82009-002_5c04b2a7-ceeb-a77b-fba1-ef8811d38669
Description

1000 TABLET, FILM COATED in 1 BOTTLE (82009-002-10)

Marketing

Marketing Status
Marketed Since 2021-11-23
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": "5c04b2a7-ceeb-a77b-fba1-ef8811d38669", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["259255", "617310", "617311", "617312"], "spl_set_id": ["f00a83aa-3f1d-566d-b9bb-f396f22a27cb"], "manufacturer_name": ["Quallent"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82009-002-10)", "package_ndc": "82009-002-10", "marketing_start_date": "20211123"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "82009-002_5c04b2a7-ceeb-a77b-fba1-ef8811d38669", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "82009-002", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Quallent", "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": "20211123", "listing_expiration_date": "20261231"}