Package 68788-7954-9
Brand: levothyroxine sodium
Generic: levothyroxine sodiumPackage Facts
Identity
Package NDC
68788-7954-9
Digits Only
6878879549
Product NDC
68788-7954
Description
90 TABLET in 1 BOTTLE (68788-7954-9)
Marketing
Marketing Status
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": "a7fe7d23-0988-429f-9d00-e3e37a3bc104", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["c38c3c31-6834-4590-ace0-f525e5599f66"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7954-3)", "package_ndc": "68788-7954-3", "marketing_start_date": "20210709"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7954-9)", "package_ndc": "68788-7954-9", "marketing_start_date": "20210709"}], "brand_name": "Levothyroxine sodium", "product_id": "68788-7954_a7fe7d23-0988-429f-9d00-e3e37a3bc104", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-7954", "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": "75 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20210709", "listing_expiration_date": "20261231"}