Package 39822-0151-1

Brand: liothyronine sodium

Generic: liothyronine sodium
NDC Package

Package Facts

Identity

Package NDC 39822-0151-1
Digits Only 3982201511
Product NDC 39822-0151
Product ID 39822-0151_02f79412-2198-a8af-e063-6394a90a0853
Description

1 VIAL in 1 CARTON (39822-0151-1) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2005-08-17
Brand liothyronine sodium
Generic liothyronine sodium
Sample Package No

Linked Drug Pages (1)

Liothyronine Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "02f79412-2198-a8af-e063-6394a90a0853", "openfda": {"unii": ["GCA9VV7D2N"], "rxcui": ["903694"], "spl_set_id": ["a8b39730-de19-497d-bde8-6594aa528403"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (39822-0151-1)  / 1 mL in 1 VIAL", "package_ndc": "39822-0151-1", "marketing_start_date": "20050817"}], "brand_name": "Liothyronine Sodium", "product_id": "39822-0151_02f79412-2198-a8af-e063-6394a90a0853", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "39822-0151", "generic_name": "Liothyronine Sodium", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "10 ug/mL"}], "application_number": "ANDA076923", "marketing_category": "ANDA", "marketing_start_date": "20050817", "listing_expiration_date": "20261231"}