Package 24201-002-01

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 24201-002-01
Digits Only 2420100201
Product NDC 24201-002
Product ID 24201-002_563fecaf-128d-4f6b-81c8-715b4d90a261
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (24201-002-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-11-15
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": ["INTRAVENOUS"], "spl_id": "563fecaf-128d-4f6b-81c8-715b4d90a261", "openfda": {"unii": ["9J765S329G"], "rxcui": ["2621123"], "spl_set_id": ["6279390b-ee61-4ef9-ac15-25537ca783c1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (24201-002-01)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "24201-002-01", "marketing_start_date": "20221115"}], "brand_name": "Levothyroxine Sodium", "product_id": "24201-002_563fecaf-128d-4f6b-81c8-715b4d90a261", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "24201-002", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/mL"}], "application_number": "NDA214253", "marketing_category": "NDA", "marketing_start_date": "20221115", "listing_expiration_date": "20261231"}