Package 82804-149-90
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
82804-149-90
Digits Only
8280414990
Product NDC
82804-149
Description
90 TABLET in 1 BOTTLE (82804-149-90)
Marketing
Marketing Status
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": "b4f8dfd0-b15a-4da5-a0d0-ad768e0b7ff8", "openfda": {"upc": ["0382804149902"], "unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["b4f8dfd0-b15a-4da5-a0d0-ad768e0b7ff8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-149-30)", "package_ndc": "82804-149-30", "marketing_start_date": "20240920"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-149-90)", "package_ndc": "82804-149-90", "marketing_start_date": "20240920"}], "brand_name": "Levothyroxine sodium", "product_id": "82804-149_b4f8dfd0-b15a-4da5-a0d0-ad768e0b7ff8", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "82804-149", "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": "ANDA207588", "marketing_category": "ANDA", "marketing_start_date": "20220921", "listing_expiration_date": "20261231"}