levothyroxine sodium

Generic: levothyroxine sodium

Labeler: xlcare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levothyroxine sodium
Generic Name levothyroxine sodium
Labeler xlcare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium .088 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72865-239
Product ID 72865-239_16376b6d-2936-4208-ab94-3e0969dce769
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215259
Listing Expiration 2026-12-31
Marketing Start 2023-01-18

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865239
Hyphenated Format 72865-239

Supplemental Identifiers

RxCUI
892246 892251 892255 966220 966221 966222 966224 966225 966248 966249 966253 966270
UPC
0372865240106 0372865242100 0372865243107 0372865241103 0372865246108 0372865245101 0372865244104 0372865237106 0372865237908 0372865247105 0372865236109 0372865239100 0372865238905 0372865238103
UNII
9J765S329G

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 (source: ndc)
Application Number ANDA215259 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • .088 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (72865-239-10)
  • 90 TABLET in 1 BOTTLE (72865-239-90)
source: ndc

Packages (2)

72865-239-10 1000 TABLET in 1 BOTTLE (72865-239-10) 72865-239-90 90 TABLET in 1 BOTTLE (72865-239-90)

Ingredients (1)

levothyroxine sodium (.088 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": "16376b6d-2936-4208-ab94-3e0969dce769", "openfda": {"upc": ["0372865240106", "0372865242100", "0372865243107", "0372865241103", "0372865246108", "0372865245101", "0372865244104", "0372865237106", "0372865237908", "0372865247105", "0372865236109", "0372865239100", "0372865238905", "0372865238103"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "892255", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["51a27110-e787-409b-98ba-c6471d0ad5cf"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72865-239-10)", "package_ndc": "72865-239-10", "marketing_start_date": "20230118"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72865-239-90)", "package_ndc": "72865-239-90", "marketing_start_date": "20230118"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72865-239_16376b6d-2936-4208-ab94-3e0969dce769", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72865-239", "generic_name": "levothyroxine sodium", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".088 mg/1"}], "application_number": "ANDA215259", "marketing_category": "ANDA", "marketing_start_date": "20230118", "listing_expiration_date": "20261231"}