levothyroxine sodium

Generic: levothyroxine sodium anhydrous

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium anhydrous
Labeler sagent pharmaceuticals
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

levothyroxine sodium anhydrous 200 ug/5mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-469
Product ID 25021-469_2662e418-ef9b-40be-abbd-db71401e3c20
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208749
Listing Expiration 2026-12-31
Marketing Start 2024-01-01

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021469
Hyphenated Format 25021-469

Supplemental Identifiers

RxCUI
966219 1115267 1115269
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 ANDA208749 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 ug/5mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (25021-469-10) / 5 mL in 1 VIAL
source: ndc

Packages (1)

25021-469-10 1 VIAL in 1 CARTON (25021-469-10) / 5 mL in 1 VIAL

Ingredients (1)

levothyroxine sodium anhydrous (200 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": "2662e418-ef9b-40be-abbd-db71401e3c20", "openfda": {"unii": ["054I36CPMN"], "rxcui": ["966219", "1115267", "1115269"], "spl_set_id": ["f57e9b19-6f17-4520-80fc-511322cc56c9"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-469-10)  / 5 mL in 1 VIAL", "package_ndc": "25021-469-10", "marketing_start_date": "20240101"}], "brand_name": "Levothyroxine Sodium", "product_id": "25021-469_2662e418-ef9b-40be-abbd-db71401e3c20", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "25021-469", "generic_name": "Levothyroxine Sodium Anhydrous", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM ANHYDROUS", "strength": "200 ug/5mL"}], "application_number": "ANDA208749", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}