Package 51655-696-52

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 51655-696-52
Digits Only 5165569652
Product NDC 51655-696
Product ID 51655-696_48722f04-d4a7-c58d-e063-6394a90a16f3
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-696-52)

Marketing

Marketing Status
Marketed Since 2021-04-01
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": "48722f04-d4a7-c58d-e063-6394a90a16f3", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966221", "966222", "966224", "966225", "966248", "966253", "966270"], "spl_set_id": ["c968836a-f94c-4d13-e053-2995a90a8df5"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-696-52)", "package_ndc": "51655-696-52", "marketing_start_date": "20210401"}], "brand_name": "Levothyroxine Sodium", "product_id": "51655-696_48722f04-d4a7-c58d-e063-6394a90a16f3", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-696", "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": ".125 mg/1"}], "application_number": "NDA021210", "marketing_category": "NDA", "marketing_start_date": "20210401", "listing_expiration_date": "20271231"}