Package 72305-137-30

Brand: euthyrox

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72305-137-30
Digits Only 7230513730
Product NDC 72305-137
Product ID 72305-137_8b98dc0b-b9fa-42eb-81a0-07b4679d9332
Description

2 BLISTER PACK in 1 CARTON (72305-137-30) / 15 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-09-30
Brand euthyrox
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

EUTHYROX ndc-match (0.95)

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 (72305-137-30)  / 15 TABLET in 1 BLISTER PACK", "package_ndc": "72305-137-30", "marketing_end_date": "20260930", "marketing_start_date": "20181017"}], "brand_name": "EUTHYROX", "product_id": "72305-137_8b98dc0b-b9fa-42eb-81a0-07b4679d9332", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72305-137", "generic_name": "levothyroxine sodium", "labeler_name": "Provell Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EUTHYROX", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "137 ug/1"}], "application_number": "NDA021292", "marketing_category": "NDA", "marketing_end_date": "20260930", "marketing_start_date": "20181017"}