Package 50090-6880-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-6880-0
Digits Only 5009068800
Product NDC 50090-6880
Description

90 TABLET in 1 BOTTLE (50090-6880-0)

Marketing

Marketing Status
Marketed Since 2023-12-05
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": "7fa57b32-b58f-4812-8b70-39c482bf9b48", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966248"], "spl_set_id": ["eb120047-a43b-40a4-9f55-067b1b51edda"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6880-0)", "package_ndc": "50090-6880-0", "marketing_start_date": "20231205"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-6880_7fa57b32-b58f-4812-8b70-39c482bf9b48", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-6880", "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": ".112 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}