Package 68788-4005-3

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-4005-3
Digits Only 6878840053
Product NDC 68788-4005
Description

30 TABLET in 1 BOTTLE (68788-4005-3)

Marketing

Marketing Status
Marketed Since 2025-08-01
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": "609352a9-740f-4874-997b-60b58d0c2b8a", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["609352a9-740f-4874-997b-60b58d0c2b8a"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-4005-3)", "package_ndc": "68788-4005-3", "marketing_start_date": "20250801"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-4005-9)", "package_ndc": "68788-4005-9", "marketing_start_date": "20250801"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "68788-4005_609352a9-740f-4874-997b-60b58d0c2b8a", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-4005", "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": "50 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250801", "listing_expiration_date": "20261231"}