Package 67046-1612-3

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 67046-1612-3
Digits Only 6704616123
Product NDC 67046-1612
Product ID 67046-1612_4302e10f-7a8b-1b53-e063-6294a90abfc0
Description

30 TABLET in 1 BLISTER PACK (67046-1612-3)

Marketing

Marketing Status
Marketed Since 2025-11-07
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": "4302e10f-7a8b-1b53-e063-6294a90abfc0", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966224"], "spl_set_id": ["4302e36f-0b5b-f645-e063-6394a90a010f"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1612-3)", "package_ndc": "67046-1612-3", "marketing_start_date": "20251107"}], "brand_name": "Levothyroxine Sodium", "product_id": "67046-1612_4302e10f-7a8b-1b53-e063-6294a90abfc0", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "67046-1612", "generic_name": "Levothyroxine Sodium", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "125 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20251107", "listing_expiration_date": "20261231"}