Package 16714-166-01

Brand: liothyronine sodium

Generic: liothyronine sodium
NDC Package

Package Facts

Identity

Package NDC 16714-166-01
Digits Only 1671416601
Product NDC 16714-166
Description

100 TABLET in 1 BOTTLE (16714-166-01)

Marketing

Marketing Status
Marketed Since 2021-05-05
Brand liothyronine sodium
Generic liothyronine sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "215d81f8-589d-490f-a470-8c50fb7aad65", "openfda": {"upc": ["0316714166018", "0316714167015"], "unii": ["GCA9VV7D2N"], "rxcui": ["903456", "903697", "903703"], "spl_set_id": ["c97dc9ec-af73-4836-aa0d-c27e66e792a9"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-166-01)", "package_ndc": "16714-166-01", "marketing_start_date": "20210505"}], "brand_name": "Liothyronine sodium", "product_id": "16714-166_215d81f8-589d-490f-a470-8c50fb7aad65", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "16714-166", "generic_name": "Liothyronine sodium", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "5 ug/1"}], "application_number": "ANDA214803", "marketing_category": "ANDA", "marketing_start_date": "20210505", "listing_expiration_date": "20261231"}