Package 51655-727-52
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
51655-727-52
Digits Only
5165572752
Product NDC
51655-727
Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-727-52)
Marketing
Marketing Status
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": "4951182c-df9e-ecd4-e063-6294a90a8afe", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966225"], "spl_set_id": ["db89c58f-9dd0-b6d6-e053-2a95a90ae2e7"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-727-52)", "package_ndc": "51655-727-52", "marketing_start_date": "20210611"}], "brand_name": "levothyroxine sodium", "product_id": "51655-727_4951182c-df9e-ecd4-e063-6294a90a8afe", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "51655-727", "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": "150 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20210611", "listing_expiration_date": "20271231"}