Package 68071-5226-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-5226-9
Digits Only 6807152269
Product NDC 68071-5226
Product ID 68071-5226_1b59050f-08e5-7b37-e063-6294a90a72cc
Description

90 TABLET in 1 BOTTLE (68071-5226-9)

Marketing

Marketing Status
Marketed Since 2020-03-30
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": "1b59050f-08e5-7b37-e063-6294a90a72cc", "openfda": {"upc": ["0368071522693"], "unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["a2157cf0-5c8f-7e69-e053-2a95a90aa083"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5226-9)", "package_ndc": "68071-5226-9", "marketing_start_date": "20200330"}], "brand_name": "levothyroxine sodium", "product_id": "68071-5226_1b59050f-08e5-7b37-e063-6294a90a72cc", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-5226", "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": "50 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}