Package 68071-5227-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-5227-9
Digits Only 6807152279
Product NDC 68071-5227
Product ID 68071-5227_1b592020-c769-2381-e063-6394a90a74b7
Description

90 TABLET in 1 BOTTLE (68071-5227-9)

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": "1b592020-c769-2381-e063-6394a90a74b7", "openfda": {"upc": ["0368071522792"], "unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["a215da96-acd9-6b8d-e053-2995a90a7e0d"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-5227-9)", "package_ndc": "68071-5227-9", "marketing_start_date": "20200330"}], "brand_name": "levothyroxine sodium", "product_id": "68071-5227_1b592020-c769-2381-e063-6394a90a74b7", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-5227", "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": "75 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}