Package 72789-084-30
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
72789-084-30
Digits Only
7278908430
Product NDC
72789-084
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-084-30)
Marketing
Marketing Status
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": "40319bfe-94c6-50ec-e063-6394a90a2912", "openfda": {"upc": ["0372789084305"], "unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["46eeb12f-7e38-4828-b7d1-26b6155bc64a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-084-30)", "package_ndc": "72789-084-30", "marketing_start_date": "20200520"}], "brand_name": "Atorvastatin calcium", "product_id": "72789-084_40319bfe-94c6-50ec-e063-6394a90a2912", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72789-084", "generic_name": "Atorvastatin calcium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA211933", "marketing_category": "ANDA", "marketing_start_date": "20190208", "listing_expiration_date": "20261231"}