pioglitazone hydrochloride
Generic: pioglitazone hydrochloride
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
pioglitazone hydrochloride
Generic Name
pioglitazone hydrochloride
Labeler
bryant ranch prepack
Dosage Form
TABLET
Routes
Active Ingredients
pioglitazone hydrochloride 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-9664
Product ID
71335-9664_7ce903c0-32c0-4eeb-8ca8-70973a7d5eb4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200268
Listing Expiration
2026-12-31
Marketing Start
2013-02-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713359664
Hyphenated Format
71335-9664
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 hydrochloride (source: ndc)
Generic Name
pioglitazone hydrochloride (source: ndc)
Application Number
ANDA200268 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (71335-9664-1)
- 60 TABLET in 1 BOTTLE (71335-9664-2)
- 90 TABLET in 1 BOTTLE (71335-9664-3)
- 180 TABLET in 1 BOTTLE (71335-9664-4)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7ce903c0-32c0-4eeb-8ca8-70973a7d5eb4", "openfda": {"unii": ["JQT35NPK6C"], "rxcui": ["312440"], "spl_set_id": ["c9548800-4c44-473d-a89b-c705484548b3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9664-1)", "package_ndc": "71335-9664-1", "marketing_start_date": "20250627"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9664-2)", "package_ndc": "71335-9664-2", "marketing_start_date": "20250627"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9664-3)", "package_ndc": "71335-9664-3", "marketing_start_date": "20230306"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-9664-4)", "package_ndc": "71335-9664-4", "marketing_start_date": "20250627"}], "brand_name": "PIOGLITAZONE HYDROCHLORIDE", "product_id": "71335-9664_7ce903c0-32c0-4eeb-8ca8-70973a7d5eb4", "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": "71335-9664", "generic_name": "pioglitazone hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PIOGLITAZONE HYDROCHLORIDE", "active_ingredients": [{"name": "PIOGLITAZONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA200268", "marketing_category": "ANDA", "marketing_start_date": "20130213", "listing_expiration_date": "20261231"}