Package 68071-3571-9

Brand: liothyronine sodium

Generic: liothyronine sodium
NDC Package

Package Facts

Identity

Package NDC 68071-3571-9
Digits Only 6807135719
Product NDC 68071-3571
Description

90 TABLET in 1 BOTTLE (68071-3571-9)

Marketing

Marketing Status
Marketed Since 2024-02-12
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": "1133ebe8-38c3-2505-e063-6294a90aaa2f", "openfda": {"upc": ["0368071357196"], "unii": ["GCA9VV7D2N"], "rxcui": ["903456"], "spl_set_id": ["1133ebe8-38c2-2505-e063-6294a90aaa2f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3571-9)", "package_ndc": "68071-3571-9", "marketing_start_date": "20240212"}], "brand_name": "Liothyronine Sodium", "product_id": "68071-3571_1133ebe8-38c3-2505-e063-6294a90aaa2f", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "68071-3571", "generic_name": "Liothyronine Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "5 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}