United States · FDA National Drug Code directory
PIOGLITAZONE HYDROCHLORIDE
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
- 76385-180_a41fecfd-4068-40ad-bc76-96c48ff32f5e
- Product NDC
- 76385-180
- Form
- TABLET
- Composition / generic term
- PIOGLITAZONE HYDROCHLORIDE
- Labeler
- Unichem Pharmaceuticals (USA), Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260625
- Source listing expiry
- 20271231
Source-listed ingredients
- PIOGLITAZONE HYDROCHLORIDE — 45 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (76385-180-10) · 76385-180-10
- 30 TABLET in 1 BOTTLE (76385-180-30) · 76385-180-30
- 500 TABLET in 1 BOTTLE (76385-180-50) · 76385-180-50
- 90 TABLET in 1 BOTTLE (76385-180-90) · 76385-180-90
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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