Package 72266-261-01

Brand: levothyroxine sodium

Generic: levothyroxine sodium anhydrous
NDC Package

Package Facts

Identity

Package NDC 72266-261-01
Digits Only 7226626101
Product NDC 72266-261
Product ID 72266-261_33611328-03f9-d3f1-e063-6394a90ad483
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (72266-261-01) / 5 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2025-09-18
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": "33611328-03f9-d3f1-e063-6394a90ad483", "openfda": {"unii": ["054I36CPMN"], "rxcui": ["1115267"], "spl_set_id": ["3361138a-6e6f-e8df-e063-6294a90af2de"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72266-261-01)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72266-261-01", "marketing_start_date": "20250918"}], "brand_name": "Levothyroxine Sodium", "product_id": "72266-261_33611328-03f9-d3f1-e063-6394a90ad483", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72266-261", "generic_name": "LEVOTHYROXINE SODIUM ANHYDROUS", "labeler_name": "Fosun Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "100 ug/5mL"}], "application_number": "ANDA216729", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}