Package 68788-7725-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7725-9
Digits Only 6878877259
Product NDC 68788-7725
Description

90 TABLET in 1 BOTTLE (68788-7725-9)

Marketing

Marketing Status
Marketed Since 2020-07-01
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": "b03c3f20-a3e1-4155-86b0-d10220f0ae5c", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["ac10b751-5195-4987-a841-400ae79730f0"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7725-3)", "package_ndc": "68788-7725-3", "marketing_start_date": "20200701"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7725-9)", "package_ndc": "68788-7725-9", "marketing_start_date": "20200701"}], "brand_name": "levothyroxine sodium", "product_id": "68788-7725_b03c3f20-a3e1-4155-86b0-d10220f0ae5c", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7725", "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": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20200701", "listing_expiration_date": "20261231"}