Package 68788-7969-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7969-9
Digits Only 6878879699
Product NDC 68788-7969
Description

90 TABLET in 1 BOTTLE (68788-7969-9)

Marketing

Marketing Status
Marketed Since 2021-07-28
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": "cac8cf0b-89b2-43dd-80cb-ede3eba51281", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966220"], "spl_set_id": ["633b3f9c-9578-4e07-a515-aec1a8b65e92"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7969-3)", "package_ndc": "68788-7969-3", "marketing_start_date": "20210728"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7969-9)", "package_ndc": "68788-7969-9", "marketing_start_date": "20210728"}], "brand_name": "Levothyroxine sodium", "product_id": "68788-7969_cac8cf0b-89b2-43dd-80cb-ede3eba51281", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7969", "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": "25 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20210728", "listing_expiration_date": "20261231"}