Package 0527-3288-46

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 0527-3288-46
Digits Only 0527328846
Product NDC 0527-3288
Description

90 TABLET in 1 BOTTLE (0527-3288-46)

Marketing

Marketing Status
Marketed Since 2020-08-03
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": "47e50f93-a701-747e-e063-6294a90a5259", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "892251", "892255", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253", "966270"], "spl_set_id": ["a8db0f7d-8863-9309-e053-2995a90a284a"], "manufacturer_name": ["Lannett Company, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (0527-3288-43)", "package_ndc": "0527-3288-43", "marketing_start_date": "20200803"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (0527-3288-46)", "package_ndc": "0527-3288-46", "marketing_start_date": "20200803"}], "brand_name": "Levothyroxine Sodium", "product_id": "0527-3288_47e50f93-a701-747e-e063-6294a90a5259", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "0527-3288", "generic_name": "Levothyroxine Sodium", "labeler_name": "Lannett Company, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "150 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20271231"}