Package 0904-6951-61

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 0904-6951-61
Digits Only 0904695161
Product NDC 0904-6951
Product ID 0904-6951_942c00a3-b31c-48d5-a63d-6d394645ee1f
Description

100 BLISTER PACK in 1 CARTON (0904-6951-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-03-20
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": "942c00a3-b31c-48d5-a63d-6d394645ee1f", "openfda": {"unii": ["9J765S329G"], "rxcui": ["892246", "966220", "966221", "966222", "966224", "966225", "966248", "966249", "966253"], "spl_set_id": ["333642fd-93ae-4dc0-9c83-6d6b163c1c74"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6951-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6951-61", "marketing_start_date": "20190320"}], "brand_name": "Levothyroxine Sodium", "product_id": "0904-6951_942c00a3-b31c-48d5-a63d-6d394645ee1f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "0904-6951", "generic_name": "Levothyroxine Sodium", "labeler_name": "Major Pharmaceuticals", "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": "20190320", "listing_expiration_date": "20261231"}