Package 72162-1462-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72162-1462-0
Digits Only 7216214620
Product NDC 72162-1462
Product ID 72162-1462_d35b5250-c26d-4d67-8a33-2f993b13e3e9
Description

1000 TABLET in 1 BOTTLE (72162-1462-0)

Marketing

Marketing Status
Marketed Since 2019-05-07
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d35b5250-c26d-4d67-8a33-2f993b13e3e9", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["d35b5250-c26d-4d67-8a33-2f993b13e3e9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1462-0)", "package_ndc": "72162-1462-0", "marketing_start_date": "20190507"}], "brand_name": "levothyroxine sodium", "product_id": "72162-1462_d35b5250-c26d-4d67-8a33-2f993b13e3e9", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72162-1462", "generic_name": "levothyroxine sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}