Package 68071-3814-3

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3814-3
Digits Only 6807138143
Product NDC 68071-3814
Product ID 68071-3814_30cce5b1-ed48-5bf2-e063-6394a90aaf1d
Description

30 TABLET in 1 BOTTLE (68071-3814-3)

Marketing

Marketing Status
Marketed Since 2025-03-20
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": "30cce5b1-ed48-5bf2-e063-6394a90aaf1d", "openfda": {"upc": ["0368071381436"], "unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["30ccec8b-3f95-61c7-e063-6394a90a05a0"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3814-3)", "package_ndc": "68071-3814-3", "marketing_start_date": "20250320"}], "brand_name": "Levothyroxine Sodium", "product_id": "68071-3814_30cce5b1-ed48-5bf2-e063-6394a90aaf1d", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-3814", "generic_name": "Levothyroxine Sodium", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": ".088 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}