EUTHYROX

Generic: levothyroxine sodium

Labeler: Provell Pharmaceuticals, LLC
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive

Drug Facts

Product Profile

Brand Name EUTHYROX
Generic Name levothyroxine sodium
Labeler Provell Pharmaceuticals, LLC
Dosage Form TABLET
Routes
ORAL
Active Ingredients

LEVOTHYROXINE SODIUM 200 ug/1

Identifiers & Regulatory

Product NDC 72305-200
Product ID 72305-200_8b98dc0b-b9fa-42eb-81a0-07b4679d9332
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021292
Marketing Start 2018-10-17
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72305200
Hyphenated Format 72305-200

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
  • 200 ug/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (72305-200-30) / 15 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

72305-200-30 2 BLISTER PACK in 1 CARTON (72305-200-30) / 15 TABLET in 1 BLISTER PACK

Ingredients (1)

LEVOTHYROXINE SODIUM (200 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 (72305-200-30)  / 15 TABLET in 1 BLISTER PACK", "package_ndc": "72305-200-30", "marketing_end_date": "20260228", "marketing_start_date": "20181017"}], "brand_name": "EUTHYROX", "product_id": "72305-200_8b98dc0b-b9fa-42eb-81a0-07b4679d9332", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72305-200", "generic_name": "levothyroxine sodium", "labeler_name": "Provell Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EUTHYROX", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "NDA021292", "marketing_category": "NDA", "marketing_end_date": "20260228", "marketing_start_date": "20181017"}