NDC 71335-9664 – Pioglitazone Hydrochloride

Pioglitazone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9664

Product details

Brand name
Pioglitazone Hydrochloride
Generic name
Pioglitazone hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA200268
Marketed since
February 13, 2013
Listing expires
December 31, 2026
Pharmacologic class
Peroxisome Proliferator Receptor alpha Agonist; Peroxisome Proliferator Receptor gamma Agonist; Thiazolidinedione

Active ingredients

Uses, dosage, side effects and warnings for Pioglitazone Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
71335-9664-130 TABLET in 1 BOTTLE (71335-9664-1)Jun 27, 2025
71335-9664-260 TABLET in 1 BOTTLE (71335-9664-2)Jun 27, 2025
71335-9664-390 TABLET in 1 BOTTLE (71335-9664-3)Mar 6, 2023
71335-9664-4180 TABLET in 1 BOTTLE (71335-9664-4)Jun 27, 2025

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