Package 70518-4402-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4402-0
Digits Only 7051844020
Product NDC 70518-4402
Product ID 70518-4402_3ab135c9-9ea8-8d16-e063-6294a90ab572
Description

90 TABLET in 1 BOTTLE (70518-4402-0)

Marketing

Marketing Status
Marketed Since 2025-07-24
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Levothyroxine sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ab135c9-9ea8-8d16-e063-6294a90ab572", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["7fd988be-ab3d-406d-a55d-1e5a8a2101cc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70518-4402-0)", "package_ndc": "70518-4402-0", "marketing_start_date": "20250724"}], "brand_name": "Levothyroxine sodium", "product_id": "70518-4402_3ab135c9-9ea8-8d16-e063-6294a90ab572", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70518-4402", "generic_name": "Levothyroxine Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "125 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20250724", "listing_expiration_date": "20261231"}