liothyronine sodium
Generic: liothyronine sodium
Labeler: sigmapharm laboratories, llcDrug Facts
Product Profile
Brand Name
liothyronine sodium
Generic Name
liothyronine sodium
Labeler
sigmapharm laboratories, llc
Dosage Form
TABLET
Routes
Active Ingredients
liothyronine sodium 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
42794-020
Product ID
42794-020_f1f181e3-ceed-1d17-e053-2995a90af5cd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200295
Listing Expiration
2026-12-31
Marketing Start
2012-12-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42794020
Hyphenated Format
42794-020
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
ANDA200295 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 100 TABLET in 1 BOTTLE (42794-020-02)
- 90 TABLET in 1 BOTTLE (42794-020-12)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f1f181e3-ceed-1d17-e053-2995a90af5cd", "openfda": {"upc": ["0342794018121", "0342794019128", "0342794020124"], "unii": ["GCA9VV7D2N"], "rxcui": ["903456", "903697", "903703"], "spl_set_id": ["38ef3766-bb9a-402e-9e4a-ad8bb5b26e4c"], "manufacturer_name": ["SIGMAPHARM LABORATORIES, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42794-020-02)", "package_ndc": "42794-020-02", "marketing_start_date": "20121203"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42794-020-12)", "package_ndc": "42794-020-12", "marketing_start_date": "20180501"}], "brand_name": "Liothyronine Sodium", "product_id": "42794-020_f1f181e3-ceed-1d17-e053-2995a90af5cd", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "42794-020", "generic_name": "Liothyronine Sodium", "labeler_name": "SIGMAPHARM LABORATORIES, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "50 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}