liothyronine sodium
Generic: liothyronine sodium
Labeler: xgen pharmaceuticals djb, inc.Drug Facts
Product Profile
Brand Name
liothyronine sodium
Generic Name
liothyronine sodium
Labeler
xgen pharmaceuticals djb, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
liothyronine sodium 10 ug/mL
Manufacturer
Identifiers & Regulatory
Product NDC
39822-0151
Product ID
39822-0151_02f79412-2198-a8af-e063-6394a90a0853
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076923
Listing Expiration
2026-12-31
Marketing Start
2005-08-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
398220151
Hyphenated Format
39822-0151
Supplemental Identifiers
RxCUI
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
ANDA076923 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 ug/mL
Packaging
- 1 VIAL in 1 CARTON (39822-0151-1) / 1 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}