Package 42708-013-30

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package Sample

Package Facts

Identity

Package NDC 42708-013-30
Digits Only 4270801330
Product NDC 42708-013
Product ID 42708-013_45b42f33-472a-dff2-e063-6394a90a379c
Description

30 TABLET, FILM COATED in 1 BOTTLE (42708-013-30)

Marketing

Marketing Status
Marketed Since 2018-03-14
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package Yes

Linked Drug Pages (1)

ATORVASTATIN CALCIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "45b42f33-472a-dff2-e063-6394a90a379c", "openfda": {"unii": ["YRZ789OWMI"], "rxcui": ["617310", "617312"], "spl_set_id": ["f7cc5704-2131-4bcb-9ff0-33a79a8167bd"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42708-013-30)", "package_ndc": "42708-013-30", "marketing_start_date": "20180314"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "42708-013_45b42f33-472a-dff2-e063-6394a90a379c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "42708-013", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "QPharma, Inc.", "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": "20120529", "listing_expiration_date": "20261231"}