Package 50090-7802-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7802-0
Digits Only 5009078020
Product NDC 50090-7802
Description

90 TABLET in 1 BOTTLE (50090-7802-0)

Marketing

Marketing Status
Marketed Since 2025-12-01
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f11fe97d-8191-45de-9bec-0e0e2b8e4032", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["d5b005e8-a88d-450b-bbc3-393d885260f5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7802-0)", "package_ndc": "50090-7802-0", "marketing_start_date": "20251201"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "50090-7802_f11fe97d-8191-45de-9bec-0e0e2b8e4032", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7802", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "137 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250408", "listing_expiration_date": "20261231"}