Package 50090-6984-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-6984-0
Digits Only 5009069840
Product NDC 50090-6984
Description

90 TABLET in 1 BOTTLE (50090-6984-0)

Marketing

Marketing Status
Marketed Since 2023-12-26
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0ea7070d-3328-482d-8801-96ad5a86ce59", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["f0680426-3581-400c-8ab5-5e6f18d0cabc"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6984-0)", "package_ndc": "50090-6984-0", "marketing_start_date": "20231226"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-6984_0ea7070d-3328-482d-8801-96ad5a86ce59", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-6984", "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": ".088 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}