Package 72162-1093-0
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
72162-1093-0
Digits Only
7216210930
Product NDC
72162-1093
Description
1000 TABLET in 1 BOTTLE (72162-1093-0)
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": "caf7825d-f434-472f-94f3-217a41255562", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966249"], "spl_set_id": ["caf7825d-f434-472f-94f3-217a41255562"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1093-0)", "package_ndc": "72162-1093-0", "marketing_start_date": "20200803"}], "brand_name": "Levothyroxine Sodium", "product_id": "72162-1093_caf7825d-f434-472f-94f3-217a41255562", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72162-1093", "generic_name": "Levothyroxine Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "175 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}