Package 70518-3274-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70518-3274-0
Digits Only 7051832740
Product NDC 70518-3274
Product ID 70518-3274_44f9bceb-7018-7859-e063-6394a90ac2cf
Description

90 TABLET in 1 BOTTLE (70518-3274-0)

Marketing

Marketing Status
Marketed Since 2021-11-23
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": "44f9bceb-7018-7859-e063-6394a90ac2cf", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["f8c14539-8ed1-406a-9b58-8ba3a7ce7ee3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70518-3274-0)", "package_ndc": "70518-3274-0", "marketing_start_date": "20211123"}], "brand_name": "Levothyroxine sodium", "product_id": "70518-3274_44f9bceb-7018-7859-e063-6394a90ac2cf", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70518-3274", "generic_name": "Levothyroxine Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "75 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20211123", "listing_expiration_date": "20261231"}