Package 50090-7767-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 50090-7767-0
Digits Only 5009077670
Product NDC 50090-7767
Product ID 50090-7767_708d1787-de34-4bc2-900e-a1fe09e621b4
Description

90 TABLET in 1 BOTTLE (50090-7767-0)

Marketing

Marketing Status
Marketed Since 2025-11-17
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "708d1787-de34-4bc2-900e-a1fe09e621b4", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["fea284d8-0514-498b-a37c-405730b5f6a2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7767-0)", "package_ndc": "50090-7767-0", "marketing_start_date": "20251117"}], "brand_name": "Levothyroxine Sodium", "product_id": "50090-7767_708d1787-de34-4bc2-900e-a1fe09e621b4", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "50090-7767", "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 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}