Package 50090-7862-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7862-0
Digits Only 5009078620
Product NDC 50090-7862
Product ID 50090-7862_88966775-272d-476f-90f3-e35741b82811
Description

90 TABLET in 1 BOTTLE (50090-7862-0)

Marketing

Marketing Status
Marketed Since 2026-01-22
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": "88966775-272d-476f-90f3-e35741b82811", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["f2bed4e7-86e9-430e-80d9-7bd7cfcf9bf5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7862-0)", "package_ndc": "50090-7862-0", "marketing_start_date": "20260122"}], "brand_name": "levothyroxine sodium", "product_id": "50090-7862_88966775-272d-476f-90f3-e35741b82811", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7862", "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": "125 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20271231"}