Package 42708-144-30
Brand: atorvastatin calcium
Generic: atorvastatin calciumPackage Facts
Identity
Package NDC
42708-144-30
Digits Only
4270814430
Product NDC
42708-144
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-144-30)
Marketing
Marketing Status
Brand
atorvastatin calcium
Generic
atorvastatin calcium
Sample Package
Yes
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4586b1ba-5c21-e661-e063-6294a90a59be", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617311"], "spl_set_id": ["c0e2a5d0-1aa3-e131-e053-2a95a90a9870"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-144-30)", "package_ndc": "42708-144-30", "marketing_start_date": "20210423"}], "brand_name": "Atorvastatin Calcium", "product_id": "42708-144_4586b1ba-5c21-e661-e063-6294a90a59be", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42708-144", "generic_name": "Atorvastatin Calcium", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atorvastatin Calcium", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA209288", "marketing_category": "ANDA", "marketing_start_date": "20181223", "listing_expiration_date": "20261231"}