Package 72189-346-90

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72189-346-90
Digits Only 7218934690
Product NDC 72189-346
Description

90 TABLET in 1 BOTTLE (72189-346-90)

Marketing

Marketing Status
Marketed Since 2022-04-19
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4c7c58-18dd-4126-e063-6294a90aff5e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["dd032289-acee-49fc-e053-2a95a90a5999"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-346-90)", "package_ndc": "72189-346-90", "marketing_start_date": "20220419"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72189-346_2c4c7c58-18dd-4126-e063-6294a90aff5e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-346", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20220419", "listing_expiration_date": "20261231"}