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 .175 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7566
Product ID 50090-7566_2c77021c-1188-4cc6-a483-0a1ed5ce4dad
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209713
Listing Expiration 2026-12-31
Marketing Start 2019-03-20

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907566
Hyphenated Format 50090-7566

Supplemental Identifiers

RxCUI
966249
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 ANDA209713 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .175 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (50090-7566-0)
source: ndc

Packages (1)

50090-7566-0 90 TABLET in 1 BOTTLE (50090-7566-0)

Ingredients (1)

levothyroxine sodium (.175 mg/1)

Linked Drug Pages (1)

Levothyroxine Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c77021c-1188-4cc6-a483-0a1ed5ce4dad", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966249"], "spl_set_id": ["b4654497-c986-4792-9b6b-0a791c7c205b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7566-0)", "package_ndc": "50090-7566-0", "marketing_start_date": "20250530"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-7566_2c77021c-1188-4cc6-a483-0a1ed5ce4dad", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7566", "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": ".175 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}