Package 59762-1206-1
Brand: liothyronine sodium
Generic: liothyronine sodiumPackage Facts
Identity
Package NDC
59762-1206-1
Digits Only
5976212061
Product NDC
59762-1206
Description
100 TABLET in 1 BOTTLE (59762-1206-1)
Marketing
Marketing Status
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 (59762-1206-1)", "package_ndc": "59762-1206-1", "marketing_start_date": "20190206"}], "brand_name": "Liothyronine Sodium", "product_id": "59762-1206_8a790175-e4e1-4257-aa5d-ce87fc9bb8c4", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "59762-1206", "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": "5 ug/1"}], "application_number": "NDA010379", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190206", "listing_expiration_date": "20261231"}