Package 59651-555-90

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 59651-555-90
Digits Only 5965155590
Product NDC 59651-555
Product ID 59651-555_c760d0cc-2245-4914-8c67-d536c41ac90f
Description

90 TABLET in 1 BOTTLE (59651-555-90)

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Levothyroxine Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c760d0cc-2245-4914-8c67-d536c41ac90f", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251", "892255", "966225", "966249", "966270"], "spl_set_id": ["c760d0cc-2245-4914-8c67-d536c41ac90f"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (59651-555-90)", "package_ndc": "59651-555-90", "marketing_start_date": "20240716"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-555-99)", "package_ndc": "59651-555-99", "marketing_start_date": "20240716"}], "brand_name": "Levothyroxine Sodium", "product_id": "59651-555_c760d0cc-2245-4914-8c67-d536c41ac90f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "59651-555", "generic_name": "Levothyroxine Sodium", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "150 ug/1"}], "application_number": "ANDA216414", "marketing_category": "ANDA", "marketing_start_date": "20240716", "listing_expiration_date": "20261231"}