Package 72189-105-90

Brand: pioglitazone

Generic: pioglitazone
NDC Package

Package Facts

Identity

Package NDC 72189-105-90
Digits Only 7218910590
Product NDC 72189-105
Description

90 TABLET in 1 BOTTLE (72189-105-90)

Marketing

Marketing Status
Marketed Since 2020-06-12
Brand pioglitazone
Generic pioglitazone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be8ed92-afbe-9ea7-e063-6294a90a5fcb", "openfda": {"unii": ["JQT35NPK6C"], "rxcui": ["312440"], "spl_set_id": ["a7e8d5a3-b0da-1d70-e053-2a95a90aa435"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-105-90)", "package_ndc": "72189-105-90", "marketing_start_date": "20200612"}], "brand_name": "PIOGLITAZONE", "product_id": "72189-105_2be8ed92-afbe-9ea7-e063-6294a90a5fcb", "dosage_form": "TABLET", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]", "Peroxisome Proliferator Receptor gamma Agonist [EPC]", "Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]", "Peroxisome Proliferator-activated Receptor gamma Agonists [MoA]", "Thiazolidinedione [EPC]", "Thiazolidinediones [CS]"], "product_ndc": "72189-105", "generic_name": "PIOGLITAZONE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PIOGLITAZONE", "active_ingredients": [{"name": "PIOGLITAZONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA200268", "marketing_category": "ANDA", "marketing_start_date": "20200612", "listing_expiration_date": "20261231"}