Package 68071-3619-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3619-9
Digits Only 6807136199
Product NDC 68071-3619
Product ID 68071-3619_1ac85666-6200-3887-e063-6394a90a105e
Description

90 TABLET in 1 BOTTLE (68071-3619-9)

Marketing

Marketing Status
Marketed Since 2024-06-13
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": "1ac85666-6200-3887-e063-6394a90a105e", "openfda": {"upc": ["0368071361995"], "unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["1ac856d1-7067-a71d-e063-6294a90acc7c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3619-9)", "package_ndc": "68071-3619-9", "marketing_start_date": "20240613"}], "brand_name": "Levothyroxine sodium", "product_id": "68071-3619_1ac85666-6200-3887-e063-6394a90a105e", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-3619", "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": "200 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201203", "listing_expiration_date": "20261231"}