Package 71335-2290-1

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2290-1
Digits Only 7133522901
Product NDC 71335-2290
Product ID 71335-2290_d4ee6454-f01d-4efe-b089-9a22f876e8c5
Description

1000 TABLET in 1 BOTTLE (71335-2290-1)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "d4ee6454-f01d-4efe-b089-9a22f876e8c5", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966253"], "spl_set_id": ["e293dd94-b523-47a2-8bed-e6d99945ee59"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2290-1)", "package_ndc": "71335-2290-1", "marketing_start_date": "20240403"}], "brand_name": "Levothyroxine Sodium", "product_id": "71335-2290_d4ee6454-f01d-4efe-b089-9a22f876e8c5", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "71335-2290", "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": "88 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}