Package 68788-7953-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-7953-9
Digits Only 6878879539
Product NDC 68788-7953
Description

90 TABLET in 1 BOTTLE (68788-7953-9)

Marketing

Marketing Status
Marketed Since 2021-07-09
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": "49acd11d-83a9-4eb9-a3c4-e239310c24c7", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966225"], "spl_set_id": ["4f40db1e-3dd9-4c7b-93e6-64f0fd10d551"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7953-3)", "package_ndc": "68788-7953-3", "marketing_start_date": "20210709"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7953-9)", "package_ndc": "68788-7953-9", "marketing_start_date": "20210709"}], "brand_name": "Levothyroxine sodium", "product_id": "68788-7953_49acd11d-83a9-4eb9-a3c4-e239310c24c7", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7953", "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": "150 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20210709", "listing_expiration_date": "20261231"}