United States · FDA National Drug Code directory

Pioglitazone

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 71335-1759_043ced29-aa7d-48fb-9567-086f00d8ff36
Product NDC: 71335-1759
Form: TABLET
Composition / generic term: Pioglitazone
Labeler: Bryant Ranch Prepack
Marketing category: ANDA
Marketing start / end (source format): 20130213
Source listing expiry: 20271231

Source-listed ingredients

PIOGLITAZONE HYDROCHLORIDE — 45 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET in 1 BOTTLE (71335-1759-1) · 71335-1759-1
90 TABLET in 1 BOTTLE (71335-1759-2) · 71335-1759-2
180 TABLET in 1 BOTTLE (71335-1759-3) · 71335-1759-3

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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