Package 68788-7764-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7764-9
Digits Only 6878877649
Product NDC 68788-7764
Product ID 68788-7764_85ff1b11-bed6-4d76-9eaf-30069151650d
Description

90 TABLET in 1 BOTTLE (68788-7764-9)

Marketing

Marketing Status
Marketed Since 2020-07-22
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": "85ff1b11-bed6-4d76-9eaf-30069151650d", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966249"], "spl_set_id": ["3519c765-2077-4f23-8644-a6242ddbf743"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7764-3)", "package_ndc": "68788-7764-3", "marketing_start_date": "20200722"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7764-9)", "package_ndc": "68788-7764-9", "marketing_start_date": "20200722"}], "brand_name": "levothyroxine sodium", "product_id": "68788-7764_85ff1b11-bed6-4d76-9eaf-30069151650d", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7764", "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": "175 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20200722", "listing_expiration_date": "20261231"}