liothyronine sodium
Generic: liothyronine sodium
Labeler: mylan pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
liothyronine sodium
Generic Name
liothyronine sodium
Labeler
mylan pharmaceuticals inc.
Dosage Form
TABLET
Routes
Active Ingredients
liothyronine sodium 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
59762-1208
Product ID
59762-1208_8a790175-e4e1-4257-aa5d-ce87fc9bb8c4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA010379
Listing Expiration
2026-12-31
Marketing Start
2019-06-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
597621208
Hyphenated Format
59762-1208
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
liothyronine sodium (source: ndc)
Generic Name
liothyronine sodium (source: ndc)
Application Number
NDA010379 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 100 TABLET in 1 BOTTLE (59762-1208-1)
Packages (1)
Ingredients (1)
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"}