Package 42023-201-01

Brand: levothyroxine sodium

Generic: levothyroxine sodium anhydrous
NDC Package

Package Facts

Identity

Package NDC 42023-201-01
Digits Only 4202320101
Product NDC 42023-201
Product ID 42023-201_7e79776a-ca4b-49a9-8bc8-131c425c0bb2
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (42023-201-01) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2011-06-24
Brand levothyroxine sodium
Generic levothyroxine sodium anhydrous
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": "7e79776a-ca4b-49a9-8bc8-131c425c0bb2", "openfda": {"upc": ["0342023201010", "0342023203014", "0342023202017"], "unii": ["054I36CPMN"], "rxcui": ["966219", "1115267", "1115269"], "spl_set_id": ["9d815416-11c9-470e-a82f-89b0bf232e12"], "manufacturer_name": ["ENDO USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (42023-201-01)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "42023-201-01", "marketing_start_date": "20110624"}], "brand_name": "Levothyroxine Sodium", "product_id": "42023-201_7e79776a-ca4b-49a9-8bc8-131c425c0bb2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "42023-201", "generic_name": "LEVOTHYROXINE SODIUM ANHYDROUS", "labeler_name": "ENDO USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "100 ug/5mL"}], "application_number": "NDA202231", "marketing_category": "NDA", "marketing_start_date": "20110624", "listing_expiration_date": "20261231"}