levothyroxine sodium

Generic: levothyroxine sodium

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 50 ug/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7562
Product ID 50090-7562_a65719a2-b274-4266-9d37-401d390f86a6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211417
Listing Expiration 2026-12-31
Marketing Start 2025-04-08

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907562
Hyphenated Format 50090-7562

Supplemental Identifiers

RxCUI
966221
UNII
9J765S329G

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 levothyroxine sodium (source: ndc)
Generic Name levothyroxine sodium (source: ndc)
Application Number ANDA211417 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7562-0)
  • 90 TABLET in 1 BOTTLE (50090-7562-1)
source: ndc

Packages (2)

Ingredients (1)

levothyroxine sodium (50 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a65719a2-b274-4266-9d37-401d390f86a6", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["247f4d1d-6e65-4f81-a377-4dd88ae16dbb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7562-0)", "package_ndc": "50090-7562-0", "marketing_start_date": "20250528"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7562-1)", "package_ndc": "50090-7562-1", "marketing_start_date": "20250528"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "50090-7562_a65719a2-b274-4266-9d37-401d390f86a6", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7562", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "50 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}