pioglitazone

Generic: pioglitazone

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name pioglitazone
Generic Name pioglitazone
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

pioglitazone hydrochloride 15 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1659
Product ID 71335-1659_c2ec028e-5710-4a4d-98b1-c8eef3b90c13
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078670
Listing Expiration 2026-12-31
Marketing Start 2013-03-01

Pharmacologic Class

Classes
ppar alpha [cs] ppar gamma [cs] peroxisome proliferator receptor alpha agonist [epc] peroxisome proliferator receptor gamma agonist [epc] peroxisome proliferator-activated receptor activity [moa] thiazolidinedione [epc] thiazolidinediones [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351659
Hyphenated Format 71335-1659

Supplemental Identifiers

RxCUI
317573
UNII
JQT35NPK6C

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 ANDA078670 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1659-1)
  • 90 TABLET in 1 BOTTLE (71335-1659-2)
  • 60 TABLET in 1 BOTTLE (71335-1659-3)
  • 120 TABLET in 1 BOTTLE (71335-1659-4)
source: ndc

Packages (4)

Ingredients (1)

pioglitazone hydrochloride (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c2ec028e-5710-4a4d-98b1-c8eef3b90c13", "openfda": {"unii": ["JQT35NPK6C"], "rxcui": ["317573"], "spl_set_id": ["fc5ea675-0eb5-42dd-a33f-46d5fda1517c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1659-1)", "package_ndc": "71335-1659-1", "marketing_start_date": "20200708"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1659-2)", "package_ndc": "71335-1659-2", "marketing_start_date": "20200708"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1659-3)", "package_ndc": "71335-1659-3", "marketing_start_date": "20200708"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1659-4)", "package_ndc": "71335-1659-4", "marketing_start_date": "20200708"}], "brand_name": "Pioglitazone", "product_id": "71335-1659_c2ec028e-5710-4a4d-98b1-c8eef3b90c13", "dosage_form": "TABLET", "pharm_class": ["PPAR alpha [CS]", "PPAR gamma [CS]", "Peroxisome Proliferator Receptor alpha Agonist [EPC]", "Peroxisome Proliferator Receptor gamma Agonist [EPC]", "Peroxisome Proliferator-activated Receptor Activity [MoA]", "Thiazolidinedione [EPC]", "Thiazolidinediones [CS]"], "product_ndc": "71335-1659", "generic_name": "pioglitazone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pioglitazone", "active_ingredients": [{"name": "PIOGLITAZONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA078670", "marketing_category": "ANDA", "marketing_start_date": "20130301", "listing_expiration_date": "20261231"}