Package 70518-4435-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70518-4435-0
Digits Only 7051844350
Product NDC 70518-4435
Product ID 70518-4435_3c30db9f-cbe5-97e5-e063-6294a90a8c4e
Description

90 TABLET in 1 BOTTLE (70518-4435-0)

Marketing

Marketing Status
Marketed Since 2025-08-12
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": "3c30db9f-cbe5-97e5-e063-6294a90a8c4e", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["9ad82faf-3734-42a1-befe-f6197b27f534"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70518-4435-0)", "package_ndc": "70518-4435-0", "marketing_start_date": "20250812"}], "brand_name": "LEVOTHYROXINE SODIUM", "product_id": "70518-4435_3c30db9f-cbe5-97e5-e063-6294a90a8c4e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70518-4435", "generic_name": "LEVOTHYROXINE SODIUM", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVOTHYROXINE SODIUM", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "75 ug/1"}], "application_number": "ANDA211417", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}