Package 68788-7698-9
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
68788-7698-9
Digits Only
6878876989
Product NDC
68788-7698
Description
90 TABLET in 1 BOTTLE (68788-7698-9)
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": "0a8d16fa-f48c-44c3-b0b4-5e16b7e59421", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["59a99739-2da5-46a7-8811-1169123bed9b"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7698-3)", "package_ndc": "68788-7698-3", "marketing_start_date": "20200401"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7698-9)", "package_ndc": "68788-7698-9", "marketing_start_date": "20200401"}], "brand_name": "levothyroxine sodium", "product_id": "68788-7698_0a8d16fa-f48c-44c3-b0b4-5e16b7e59421", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7698", "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": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20200401", "listing_expiration_date": "20271231"}