Package 63629-2090-1

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 63629-2090-1
Digits Only 6362920901
Product NDC 63629-2090
Description

1000 TABLET in 1 BOTTLE (63629-2090-1)

Marketing

Marketing Status
Marketed Since 2021-02-09
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": "69fb5cd6-90ba-487d-a754-07c664a1fdd1", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966249"], "spl_set_id": ["69fb5cd6-90ba-487d-a754-07c664a1fdd1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-2090-1)", "package_ndc": "63629-2090-1", "marketing_start_date": "20210209"}], "brand_name": "Levothyroxine Sodium", "product_id": "63629-2090_69fb5cd6-90ba-487d-a754-07c664a1fdd1", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "63629-2090", "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": "175 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}