Package 68071-2278-9

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-2278-9
Digits Only 6807122789
Product NDC 68071-2278
Product ID 68071-2278_1d7815c7-abd3-9fbd-e063-6394a90a11f7
Description

90 TABLET in 1 BOTTLE (68071-2278-9)

Marketing

Marketing Status
Marketed Since 2020-10-15
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": "1d7815c7-abd3-9fbd-e063-6394a90a11f7", "openfda": {"upc": ["0368071227895"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["b1b8c5a4-8132-24d2-e053-2995a90a59ec"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-2278-9)", "package_ndc": "68071-2278-9", "marketing_start_date": "20201015"}], "brand_name": "Levothyroxine Sodium", "product_id": "68071-2278_1d7815c7-abd3-9fbd-e063-6394a90a11f7", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "68071-2278", "generic_name": "Levothyroxine Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}