levothyroxine sodium

Generic: levothyroxine sodium anhydrous

Labeler: fosun pharma usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium anhydrous
Labeler fosun pharma usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

levothyroxine sodium anhydrous 100 ug/5mL

Manufacturer
Fosun Pharma USA Inc.

Identifiers & Regulatory

Product NDC 72266-261
Product ID 72266-261_33611328-03f9-d3f1-e063-6394a90ad483
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216729
Listing Expiration 2026-12-31
Marketing Start 2025-09-18

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72266261
Hyphenated Format 72266-261

Supplemental Identifiers

RxCUI
1115267
UNII
054I36CPMN

Packaging Origin

Original Packager
true

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 anhydrous (source: ndc)
Application Number ANDA216729 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 100 ug/5mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (72266-261-01) / 5 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

72266-261-01 1 VIAL, SINGLE-DOSE in 1 CARTON (72266-261-01) / 5 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

levothyroxine sodium anhydrous (100 ug/5mL)

Linked Drug Pages (1)

Levothyroxine Sodium ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "33611328-03f9-d3f1-e063-6394a90ad483", "openfda": {"unii": ["054I36CPMN"], "rxcui": ["1115267"], "spl_set_id": ["3361138a-6e6f-e8df-e063-6294a90af2de"], "manufacturer_name": ["Fosun Pharma USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (72266-261-01)  / 5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72266-261-01", "marketing_start_date": "20250918"}], "brand_name": "Levothyroxine Sodium", "product_id": "72266-261_33611328-03f9-d3f1-e063-6394a90ad483", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72266-261", "generic_name": "LEVOTHYROXINE SODIUM ANHYDROUS", "labeler_name": "Fosun Pharma USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "100 ug/5mL"}], "application_number": "ANDA216729", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}