Package 68788-8806-9
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
68788-8806-9
Digits Only
6878888069
Product NDC
68788-8806
Description
90 TABLET in 1 BOTTLE (68788-8806-9)
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": "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 (68788-8806-3)", "package_ndc": "68788-8806-3", "marketing_start_date": "20250120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8806-9)", "package_ndc": "68788-8806-9", "marketing_start_date": "20250120"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "68788-8806_7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-8806", "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": "75 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}