Package 72189-604-90

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72189-604-90
Digits Only 7218960490
Product NDC 72189-604
Product ID 72189-604_2b4bbe49-4bd1-ba16-e063-6394a90acefc
Description

90 TABLET in 1 BOTTLE (72189-604-90)

Marketing

Marketing Status
Marketed Since 2025-01-09
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": "2b4bbe49-4bd1-ba16-e063-6394a90acefc", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["2b4bbe49-4bd0-ba16-e063-6394a90acefc"], "manufacturer_name": ["Direct_rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-604-90)", "package_ndc": "72189-604-90", "marketing_start_date": "20250109"}], "brand_name": "Levothyroxine Sodium", "product_id": "72189-604_2b4bbe49-4bd1-ba16-e063-6394a90acefc", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-604", "generic_name": "Levothyroxine Sodium", "labeler_name": "Direct_rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "88 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20250109", "listing_expiration_date": "20261231"}