Package 50090-7609-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7609-0
Digits Only 5009076090
Product NDC 50090-7609
Description

90 TABLET in 1 BOTTLE (50090-7609-0)

Marketing

Marketing Status
Marketed Since 2025-07-21
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": "499f93f1-914f-4df8-8eae-82f70e92f1a3", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["cfab474d-3272-41fd-a8ec-762dd1a84fa6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7609-0)", "package_ndc": "50090-7609-0", "marketing_start_date": "20250721"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "50090-7609_499f93f1-914f-4df8-8eae-82f70e92f1a3", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7609", "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": "88 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}