pioglitazone
Generic: pioglitazone
Labeler: direct rxDrug Facts
Product Profile
Brand Name
pioglitazone
Generic Name
pioglitazone
Labeler
direct rx
Dosage Form
TABLET
Routes
Active Ingredients
pioglitazone hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72189-105
Product ID
72189-105_2be8ed92-afbe-9ea7-e063-6294a90a5fcb
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200268
Listing Expiration
2026-12-31
Marketing Start
2020-06-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72189105
Hyphenated Format
72189-105
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
pioglitazone (source: ndc)
Generic Name
pioglitazone (source: ndc)
Application Number
ANDA200268 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (72189-105-90)
Packages (1)
Ingredients (1)
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"}