Package 72162-1091-0

Brand: levothyroxine sodium

Generic: levothyroxine sodium
NDC Package

Package Facts

Identity

Package NDC 72162-1091-0
Digits Only 7216210910
Product NDC 72162-1091
Product ID 72162-1091_ef7bc627-d37b-470e-b8f7-3c472c930d05
Description

1000 TABLET in 1 BOTTLE (72162-1091-0)

Marketing

Marketing Status
Marketed Since 2020-08-03
Brand levothyroxine sodium
Generic levothyroxine sodium
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ef7bc627-d37b-470e-b8f7-3c472c930d05", "openfda": {"unii": ["9J765S329G"], "rxcui": ["966248"], "spl_set_id": ["ef7bc627-d37b-470e-b8f7-3c472c930d05"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1091-0)", "package_ndc": "72162-1091-0", "marketing_start_date": "20200803"}], "brand_name": "Levothyroxine Sodium", "product_id": "72162-1091_ef7bc627-d37b-470e-b8f7-3c472c930d05", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72162-1091", "generic_name": "Levothyroxine Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine Sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "112 ug/1"}], "application_number": "NDA021342", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20200803", "listing_expiration_date": "20261231"}