Package 70518-4401-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4401-0
Digits Only 7051844010
Product NDC 70518-4401
Product ID 70518-4401_3ab135c9-9e73-8d16-e063-6294a90ab572
Description

90 TABLET in 1 BOTTLE (70518-4401-0)

Marketing

Marketing Status
Marketed Since 2025-07-24
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": "3ab135c9-9e73-8d16-e063-6294a90ab572", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["6f25cbb3-0358-4778-b8f0-f76479a2dcc5"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70518-4401-0)", "package_ndc": "70518-4401-0", "marketing_start_date": "20250724"}], "brand_name": "Levothyroxine sodium", "product_id": "70518-4401_3ab135c9-9e73-8d16-e063-6294a90ab572", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70518-4401", "generic_name": "Levothyroxine Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20250724", "listing_expiration_date": "20261231"}