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 200 ug/1

Manufacturer
Direct Rx

Identifiers & Regulatory

Product NDC 72189-346
Product ID 72189-346_2c4c7c58-18dd-4126-e063-6294a90aff5e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212399
Listing Expiration 2026-12-31
Marketing Start 2022-04-19

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189346
Hyphenated Format 72189-346

Supplemental Identifiers

RxCUI
892251
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
  • 200 ug/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (72189-346-90)
source: ndc

Packages (1)

72189-346-90 90 TABLET in 1 BOTTLE (72189-346-90)

Ingredients (1)

levothyroxine sodium (200 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": "2c4c7c58-18dd-4126-e063-6294a90aff5e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["dd032289-acee-49fc-e053-2a95a90a5999"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-346-90)", "package_ndc": "72189-346-90", "marketing_start_date": "20220419"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72189-346_2c4c7c58-18dd-4126-e063-6294a90aff5e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72189-346", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20220419", "listing_expiration_date": "20261231"}