Package 59762-1208-1

Brand: liothyronine sodium

Generic: liothyronine sodium
NDC Package

Package Facts

Identity

Package NDC 59762-1208-1
Digits Only 5976212081
Product NDC 59762-1208
Description

100 TABLET in 1 BOTTLE (59762-1208-1)

Marketing

Marketing Status
Marketed Since 2019-06-24
Brand liothyronine sodium
Generic liothyronine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8a790175-e4e1-4257-aa5d-ce87fc9bb8c4", "openfda": {"upc": ["0359762120618"], "unii": ["GCA9VV7D2N"], "rxcui": ["903456", "903697", "903703"], "spl_set_id": ["115a84c2-0126-4dd7-816e-1873875f1e49"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59762-1208-1)", "package_ndc": "59762-1208-1", "marketing_start_date": "20190624"}], "brand_name": "Liothyronine Sodium", "product_id": "59762-1208_8a790175-e4e1-4257-aa5d-ce87fc9bb8c4", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "59762-1208", "generic_name": "liothyronine sodium", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "50 ug/1"}], "application_number": "NDA010379", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190624", "listing_expiration_date": "20261231"}