Package 63629-8712-1

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 63629-8712-1
Digits Only 6362987121
Product NDC 63629-8712
Description

1000 TABLET in 1 BOTTLE (63629-8712-1)

Marketing

Marketing Status
Marketed Since 2021-08-19
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": "addf881a-35d3-4c0b-adb2-fcb7f45b9e36", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["c22af2e0-fb36-4645-a911-3d293af5bd88"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-8712-1)", "package_ndc": "63629-8712-1", "marketing_start_date": "20210819"}], "brand_name": "levothyroxine sodium", "product_id": "63629-8712_addf881a-35d3-4c0b-adb2-fcb7f45b9e36", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "63629-8712", "generic_name": "levothyroxine sodium", "labeler_name": "Bryant Ranch Prepack", "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": "20190507", "listing_expiration_date": "20261231"}