euthyrox

Generic: levothyroxine sodium

Labeler: provell pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name euthyrox
Generic Name levothyroxine sodium
Labeler provell pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levothyroxine sodium 25 ug/1

Manufacturer
Provell Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 72305-025
Product ID 72305-025_8b98dc0b-b9fa-42eb-81a0-07b4679d9332
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021292
Marketing Start 2018-10-17
Marketing End 2026-08-31

Pharmacologic Class

Classes
thyroxine [cs] l-thyroxine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72305025
Hyphenated Format 72305-025

Supplemental Identifiers

RxCUI
892246 892251 966153 966160 966166 966173 966177 966182 966187 966196 966202 966207 966220 966221 966222 966224 966225 966248 966249 966253 966270 2104866
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 euthyrox (source: ndc)
Generic Name levothyroxine sodium (source: ndc)
Application Number NDA021292 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 ug/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (72305-025-30) / 15 TABLET in 1 BLISTER PACK
  • 6 BLISTER PACK in 1 CARTON (72305-025-90) / 15 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

72305-025-30 2 BLISTER PACK in 1 CARTON (72305-025-30) / 15 TABLET in 1 BLISTER PACK 72305-025-90 6 BLISTER PACK in 1 CARTON (72305-025-90) / 15 TABLET in 1 BLISTER PACK

Ingredients (1)

levothyroxine sodium (25 ug/1)

Linked Drug Pages (1)

EUTHYROX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8b98dc0b-b9fa-42eb-81a0-07b4679d9332", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "892251", "966153", "966160", "966166", "966173", "966177", "966182", "966187", "966196", "966202", "966207", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270", "2104866"], "spl_set_id": ["bc3c6830-ba68-4ba3-9896-a12d0ad0b275"], "manufacturer_name": ["Provell Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72305-025-30)  / 15 TABLET in 1 BLISTER PACK", "package_ndc": "72305-025-30", "marketing_end_date": "20260831", "marketing_start_date": "20181017"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (72305-025-90)  / 15 TABLET in 1 BLISTER PACK", "package_ndc": "72305-025-90", "marketing_end_date": "20260331", "marketing_start_date": "20230101"}], "brand_name": "EUTHYROX", "product_id": "72305-025_8b98dc0b-b9fa-42eb-81a0-07b4679d9332", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72305-025", "generic_name": "levothyroxine sodium", "labeler_name": "Provell Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EUTHYROX", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "25 ug/1"}], "application_number": "NDA021292", "marketing_category": "NDA", "marketing_end_date": "20260831", "marketing_start_date": "20181017"}