Package 50090-7563-0
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
50090-7563-0
Digits Only
5009075630
Product NDC
50090-7563
Description
90 TABLET in 1 BOTTLE (50090-7563-0)
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": "e20e1904-abd8-4c36-86f5-41d2c549a5c2", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["70dddaf0-f495-495f-95de-36e9efa2e373"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7563-0)", "package_ndc": "50090-7563-0", "marketing_start_date": "20250528"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "50090-7563_e20e1904-abd8-4c36-86f5-41d2c549a5c2", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7563", "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": "50 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}