Package 82804-099-90

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 82804-099-90
Digits Only 8280409990
Product NDC 82804-099
Description

90 TABLET in 1 BOTTLE (82804-099-90)

Marketing

Marketing Status
Marketed Since 2024-05-01
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": "9e69af45-d5a3-4986-8ea5-dee9e59272d7", "openfda": {"upc": ["0382804099306"], "unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["e1b322a6-9161-45b9-bf77-3c44502d5efd"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-099-30)", "package_ndc": "82804-099-30", "marketing_start_date": "20240425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-099-90)", "package_ndc": "82804-099-90", "marketing_start_date": "20240501"}], "brand_name": "Levothyroxine Sodium", "product_id": "82804-099_9e69af45-d5a3-4986-8ea5-dee9e59272d7", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82804-099", "generic_name": "Levothyroxine Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "50 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}