Package 71335-2287-1

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2287-1
Digits Only 7133522871
Product NDC 71335-2287
Product ID 71335-2287_ffd97ffd-42d4-44fb-a890-8ab7b18b36bd
Description

1000 TABLET in 1 BOTTLE (71335-2287-1)

Marketing

Marketing Status
Marketed Since 2024-05-02
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": "ffd97ffd-42d4-44fb-a890-8ab7b18b36bd", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966220"], "spl_set_id": ["8849620a-5e8d-4031-884f-9a2817b050f2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2287-1)", "package_ndc": "71335-2287-1", "marketing_start_date": "20240502"}], "brand_name": "levothyroxine sodium", "product_id": "71335-2287_ffd97ffd-42d4-44fb-a890-8ab7b18b36bd", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "71335-2287", "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": "25 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20190507", "listing_expiration_date": "20261231"}