liothyronine sodium
Generic: liothyronine sodium
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
liothyronine sodium
Generic Name
liothyronine sodium
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
liothyronine sodium 5 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-3131
Product ID
50090-3131_b001b18d-9985-47dd-983d-9a6e8522c7d7
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
500903131
Hyphenated Format
50090-3131
Supplemental Identifiers
RxCUI
UNII
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
- 5 ug/1
Packaging
- 100 TABLET in 1 BOTTLE (50090-3131-0)
- 90 TABLET in 1 BOTTLE (50090-3131-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b001b18d-9985-47dd-983d-9a6e8522c7d7", "openfda": {"unii": ["GCA9VV7D2N"], "rxcui": ["903456"], "spl_set_id": ["db65bcd8-e9c9-4095-9975-03be1f443823"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-3131-0)", "package_ndc": "50090-3131-0", "marketing_start_date": "20170905"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-3131-1)", "package_ndc": "50090-3131-1", "marketing_start_date": "20180312"}], "brand_name": "Liothyronine Sodium", "product_id": "50090-3131_b001b18d-9985-47dd-983d-9a6e8522c7d7", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "50090-3131", "generic_name": "Liothyronine Sodium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "5 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}