Package 68788-8807-3

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8807-3
Digits Only 6878888073
Product NDC 68788-8807
Description

30 TABLET in 1 BOTTLE (68788-8807-3)

Marketing

Marketing Status
Marketed Since 2025-01-20
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": "7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "966222", "966249"], "spl_set_id": ["7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8807-3)", "package_ndc": "68788-8807-3", "marketing_start_date": "20250120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8807-9)", "package_ndc": "68788-8807-9", "marketing_start_date": "20250120"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "68788-8807_7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-8807", "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": "100 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}