Package 51655-714-52

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 51655-714-52
Digits Only 5165571452
Product NDC 51655-714
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-714-52)

Marketing

Marketing Status
Marketed Since 2021-05-26
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4950fdd9-cc2c-be63-e063-6294a90a8ac9", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966249"], "spl_set_id": ["db5dd9d2-4f96-25d0-e053-2995a90af9dc"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-714-52)", "package_ndc": "51655-714-52", "marketing_start_date": "20210526"}], "brand_name": "levothyroxine sodium", "product_id": "51655-714_4950fdd9-cc2c-be63-e063-6294a90a8ac9", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-714", "generic_name": "levothyroxine sodium", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "175 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20210526", "listing_expiration_date": "20271231"}