Package 68788-8896-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68788-8896-9
Digits Only 6878888969
Product NDC 68788-8896
Product ID 68788-8896_884f9fa1-58aa-4ff7-934f-106a0470e747
Description

90 TABLET in 1 BOTTLE (68788-8896-9)

Marketing

Marketing Status
Marketed Since 2025-07-03
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": "884f9fa1-58aa-4ff7-934f-106a0470e747", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966222"], "spl_set_id": ["884f9fa1-58aa-4ff7-934f-106a0470e747"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8896-3)", "package_ndc": "68788-8896-3", "marketing_start_date": "20250703"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8896-9)", "package_ndc": "68788-8896-9", "marketing_start_date": "20250703"}], "brand_name": "Levothyroxine Sodium", "product_id": "68788-8896_884f9fa1-58aa-4ff7-934f-106a0470e747", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68788-8896", "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": ".075 mg/1"}], "application_number": "ANDA209713", "marketing_category": "ANDA", "marketing_start_date": "20250703", "listing_expiration_date": "20261231"}