Package 82804-222-30

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 82804-222-30
Digits Only 8280422230
Product NDC 82804-222
Description

30 TABLET in 1 BOTTLE (82804-222-30)

Marketing

Marketing Status
Marketed Since 2025-08-19
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": "d010d2e7-ebbe-496a-a65c-5c7c95ceb9ca", "openfda": {"upc": ["0382804222902"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["9e588c43-b9b5-478e-99f7-e197add3cd26"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-222-30)", "package_ndc": "82804-222-30", "marketing_start_date": "20250819"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-222-90)", "package_ndc": "82804-222-90", "marketing_start_date": "20250424"}], "brand_name": "Levothyroxine Sodium", "product_id": "82804-222_d010d2e7-ebbe-496a-a65c-5c7c95ceb9ca", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82804-222", "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": "100 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}