Package 68071-3717-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3717-9
Digits Only 6807137179
Product NDC 68071-3717
Product ID 68071-3717_2646aad3-40b8-1df0-e063-6294a90aed7d
Description

90 TABLET in 1 BOTTLE (68071-3717-9)

Marketing

Marketing Status
Marketed Since 2024-11-06
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": "2646aad3-40b8-1df0-e063-6294a90aed7d", "openfda": {"upc": ["0368071371796"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["2646a481-09a5-af6a-e063-6394a90a16da"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3717-9)", "package_ndc": "68071-3717-9", "marketing_start_date": "20241106"}], "brand_name": "Levothyroxine Sodium", "product_id": "68071-3717_2646aad3-40b8-1df0-e063-6294a90aed7d", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-3717", "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": ".1 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20190320", "listing_expiration_date": "20261231"}