Package 68788-8902-3

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8902-3
Digits Only 6878889023
Product NDC 68788-8902
Product ID 68788-8902_64aaeba7-1013-44a4-96fc-b876016897b3
Description

30 TABLET in 1 BOTTLE (68788-8902-3)

Marketing

Marketing Status
Marketed Since 2025-07-25
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Levothyroxine sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "64aaeba7-1013-44a4-96fc-b876016897b3", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["64aaeba7-1013-44a4-96fc-b876016897b3"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8902-3)", "package_ndc": "68788-8902-3", "marketing_start_date": "20250725"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8902-9)", "package_ndc": "68788-8902-9", "marketing_start_date": "20250725"}], "brand_name": "Levothyroxine sodium", "product_id": "68788-8902_64aaeba7-1013-44a4-96fc-b876016897b3", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-8902", "generic_name": "Levothyroxine sodium", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "ANDA207588", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}