Package 51655-128-52

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 51655-128-52
Digits Only 5165512852
Product NDC 51655-128
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-128-52)

Marketing

Marketing Status
Marketed Since 2023-03-06
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": "48c3da8c-6744-58df-e063-6394a90af2a4", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966270"], "spl_set_id": ["f6c92836-95e1-1402-e053-6394a90a2f5e"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-128-52)", "package_ndc": "51655-128-52", "marketing_start_date": "20230306"}], "brand_name": "Levothyroxine Sodium", "product_id": "51655-128_48c3da8c-6744-58df-e063-6394a90af2a4", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-128", "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": "137 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230306", "listing_expiration_date": "20271231"}