Package 68788-7704-3

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7704-3
Digits Only 6878877043
Product NDC 68788-7704
Product ID 68788-7704_35c7fe49-c864-4bff-a046-46fe267de44d
Description

30 TABLET in 1 BOTTLE (68788-7704-3)

Marketing

Marketing Status
Marketed Since 2020-05-01
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": "35c7fe49-c864-4bff-a046-46fe267de44d", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892251"], "spl_set_id": ["eb53dc23-8337-497e-b466-192f905563ed"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7704-3)", "package_ndc": "68788-7704-3", "marketing_start_date": "20200501"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7704-9)", "package_ndc": "68788-7704-9", "marketing_start_date": "20200501"}], "brand_name": "levothyroxine sodium", "product_id": "68788-7704_35c7fe49-c864-4bff-a046-46fe267de44d", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7704", "generic_name": "levothyroxine sodium", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "200 ug/1"}], "application_number": "NDA021116", "marketing_category": "NDA", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}