Package 72162-1092-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72162-1092-0
Digits Only 7216210920
Product NDC 72162-1092
Product ID 72162-1092_d6ce9798-7204-41df-9aeb-067000cb0895
Description

1000 TABLET in 1 BOTTLE (72162-1092-0)

Marketing

Marketing Status
Marketed Since 2020-08-03
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Levothyroxine Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d6ce9798-7204-41df-9aeb-067000cb0895", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["d6ce9798-7204-41df-9aeb-067000cb0895"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1092-0)", "package_ndc": "72162-1092-0", "marketing_start_date": "20200803"}], "brand_name": "Levothyroxine Sodium", "product_id": "72162-1092_d6ce9798-7204-41df-9aeb-067000cb0895", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72162-1092", "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": "137 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}