Package 71610-022-45

Brand: atorvastatin calcium

Generic: atorvastatin calcium
NDC Package

Package Facts

Identity

Package NDC 71610-022-45
Digits Only 7161002245
Product NDC 71610-022
Product ID 71610-022_eb3a5903-a3fa-4071-8e0b-38edfb013464
Description

45 TABLET, FILM COATED in 1 BOTTLE (71610-022-45)

Marketing

Marketing Status
Marketed Since 2017-12-20
Brand atorvastatin calcium
Generic atorvastatin calcium
Sample Package No

Linked Drug Pages (1)

ATORVASTATIN CALCIUM ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eb3a5903-a3fa-4071-8e0b-38edfb013464", "openfda": {"unii": ["48A5M73Z4Q"], "rxcui": ["617310"], "spl_set_id": ["c0b4f1a2-0082-4150-8f2b-e7440252b675"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (71610-022-45)", "package_ndc": "71610-022-45", "marketing_start_date": "20171220"}], "brand_name": "ATORVASTATIN CALCIUM", "product_id": "71610-022_eb3a5903-a3fa-4071-8e0b-38edfb013464", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["HMG-CoA Reductase Inhibitor [EPC]", "Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]"], "product_ndc": "71610-022", "generic_name": "ATORVASTATIN CALCIUM", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATORVASTATIN CALCIUM", "active_ingredients": [{"name": "ATORVASTATIN CALCIUM TRIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA090548", "marketing_category": "ANDA", "marketing_start_date": "20120529", "listing_expiration_date": "20261231"}