Package 70518-3154-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 70518-3154-0
Digits Only 7051831540
Product NDC 70518-3154
Product ID 70518-3154_44ab22c4-621a-52e5-e063-6294a90abfba
Description

90 TABLET in 1 BOTTLE (70518-3154-0)

Marketing

Marketing Status
Marketed Since 2021-07-14
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": "44ab22c4-621a-52e5-e063-6294a90abfba", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["55cebc88-0514-4940-b974-ec7f0467d10e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (70518-3154-0)", "package_ndc": "70518-3154-0", "marketing_start_date": "20210714"}], "brand_name": "Levothyroxine sodium", "product_id": "70518-3154_44ab22c4-621a-52e5-e063-6294a90abfba", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "70518-3154", "generic_name": "Levothyroxine Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "88 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20210714", "listing_expiration_date": "20261231"}