Package 50090-7566-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7566-0
Digits Only 5009075660
Product NDC 50090-7566
Product ID 50090-7566_2c77021c-1188-4cc6-a483-0a1ed5ce4dad
Description

90 TABLET in 1 BOTTLE (50090-7566-0)

Marketing

Marketing Status
Marketed Since 2025-05-30
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": "2c77021c-1188-4cc6-a483-0a1ed5ce4dad", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966249"], "spl_set_id": ["b4654497-c986-4792-9b6b-0a791c7c205b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7566-0)", "package_ndc": "50090-7566-0", "marketing_start_date": "20250530"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-7566_2c77021c-1188-4cc6-a483-0a1ed5ce4dad", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7566", "generic_name": "Levothyroxine Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".175 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}