Package 72603-668-01

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72603-668-01
Digits Only 7260366801
Product NDC 72603-668
Description

90 TABLET in 1 BOTTLE (72603-668-01)

Marketing

Marketing Status
Marketed Since 2025-04-08
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e51d8ca0-2d22-4390-ba97-f0075e7cc256", "openfda": {"upc": ["0372603667011", "0372603665017"], "unii": ["9J765S329G"], "rxcui": ["892246", "892251", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["58f4dc90-3648-49dc-a7e1-baf918a773b5"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72603-668-01)", "package_ndc": "72603-668-01", "marketing_start_date": "20250408"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (72603-668-02)", "package_ndc": "72603-668-02", "marketing_start_date": "20250408"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "72603-668_e51d8ca0-2d22-4390-ba97-f0075e7cc256", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72603-668", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "150 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}