Package 68788-8574-9
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
68788-8574-9
Digits Only
6878885749
Product NDC
68788-8574
Description
90 TABLET, FILM COATED in 1 BOTTLE (68788-8574-9)
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": "77075b2f-d10f-4fbf-bfae-ab5971aa6c4b", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["2d9cb8d9-b367-464d-9bcd-6de8de2b6c23"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8574-9)", "package_ndc": "68788-8574-9", "marketing_start_date": "20240126"}], "brand_name": "Atorvastatin Calcium", "product_id": "68788-8574_77075b2f-d10f-4fbf-bfae-ab5971aa6c4b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "68788-8574", "generic_name": "atorvastatin calcium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA216436", "marketing_category": "ANDA", "marketing_start_date": "20240126", "listing_expiration_date": "20261231"}