Package 72189-605-90

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72189-605-90
Digits Only 7218960590
Product NDC 72189-605
Product ID 72189-605_2b361866-e982-567c-e063-6294a90a5a5c
Description

90 TABLET in 1 BOTTLE (72189-605-90)

Marketing

Marketing Status
Marketed Since 2025-01-08
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": "2b361866-e982-567c-e063-6294a90a5a5c", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966248"], "spl_set_id": ["2b361866-e981-567c-e063-6294a90a5a5c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-605-90)", "package_ndc": "72189-605-90", "marketing_start_date": "20250108"}], "brand_name": "Levothyroxine Sodium", "product_id": "72189-605_2b361866-e982-567c-e063-6294a90a5a5c", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-605", "generic_name": "Levothyroxine Sodium", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "112 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20250108", "listing_expiration_date": "20261231"}