Package 43063-884-30

Brand: liothyronine sodium

Generic: liothyronine sodium
NDC Package

Package Facts

Identity

Package NDC 43063-884-30
Digits Only 4306388430
Product NDC 43063-884
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-884-30)

Marketing

Marketing Status
Marketed Since 2018-08-16
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": "415c6ae0-9636-3fb9-e063-6394a90accdc", "openfda": {"upc": ["0343063884300"], "unii": ["GCA9VV7D2N"], "rxcui": ["903697"], "spl_set_id": ["76fa4eb6-fefa-4e97-9543-f81e465743e6"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-884-30)", "package_ndc": "43063-884-30", "marketing_start_date": "20180816"}], "brand_name": "Liothyronine Sodium", "product_id": "43063-884_415c6ae0-9636-3fb9-e063-6394a90accdc", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "43063-884", "generic_name": "Liothyronine Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "25 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}