Package 72189-226-30
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
72189-226-30
Digits Only
7218922630
Product NDC
72189-226
Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-226-30)
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": "2c283f9f-1dbb-4a4c-e063-6394a90a7953", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617312"], "spl_set_id": ["c3b70f79-45a3-0869-e053-2a95a90a3cdb"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-226-30)", "package_ndc": "72189-226-30", "marketing_start_date": "20210601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-226-90)", "package_ndc": "72189-226-90", "marketing_start_date": "20210601"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "72189-226_2c283f9f-1dbb-4a4c-e063-6394a90a7953", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "72189-226", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA076477", "marketing_category": "ANDA", "marketing_start_date": "20210601", "listing_expiration_date": "20261231"}