Package 51655-723-52

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 51655-723-52
Digits Only 5165572352
Product NDC 51655-723
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-723-52)

Marketing

Marketing Status
Marketed Since 2021-06-09
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": "49511675-a6e5-2e5a-e063-6394a90a1007", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["c9f4923e-5625-1d4f-e053-2a95a90aabc9"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-723-52)", "package_ndc": "51655-723-52", "marketing_start_date": "20210609"}], "brand_name": "levothyroxine sodium", "product_id": "51655-723_49511675-a6e5-2e5a-e063-6394a90a1007", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-723", "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": "50 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20210609", "listing_expiration_date": "20271231"}