Package 50090-6825-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-6825-0
Digits Only 5009068250
Product NDC 50090-6825
Description

90 TABLET in 1 BOTTLE (50090-6825-0)

Marketing

Marketing Status
Marketed Since 2023-11-20
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": "294860ce-8848-484c-8288-539fe71cd240", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["99df68ea-4de7-4825-a6d7-894c70d01c28"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6825-0)", "package_ndc": "50090-6825-0", "marketing_start_date": "20231120"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-6825_294860ce-8848-484c-8288-539fe71cd240", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-6825", "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": ".075 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20271231"}