levothyroxine sodium

Generic: levothyroxine sodium

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 112 ug/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-605
Product ID 72189-605_2b361866-e982-567c-e063-6294a90a5a5c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212399
Listing Expiration 2026-12-31
Marketing Start 2025-01-08

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189605
Hyphenated Format 72189-605

Supplemental Identifiers

RxCUI
966248
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 ANDA212399 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 112 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (72189-605-90)
source: ndc

Packages (1)

72189-605-90 90 TABLET in 1 BOTTLE (72189-605-90)

Ingredients (1)

levothyroxine sodium (112 ug/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": "2b361866-e982-567c-e063-6294a90a5a5c", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966248"], "spl_set_id": ["2b361866-e981-567c-e063-6294a90a5a5c"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-605-90)", "package_ndc": "72189-605-90", "marketing_start_date": "20250108"}], "brand_name": "Levothyroxine Sodium", "product_id": "72189-605_2b361866-e982-567c-e063-6294a90a5a5c", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-605", "generic_name": "Levothyroxine Sodium", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "112 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20250108", "listing_expiration_date": "20261231"}