United States · FDA National Drug Code directory

Pioglitazone Hydrochloride and Metformin 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
57237-218_e1c4f0ca-4474-4bac-8884-8180e7aec050
Product NDC
57237-218
Form
TABLET, FILM COATED
Composition / generic term
Pioglitazone Hydrochloride and Metformin Hydrochloride
Labeler
Rising Pharma Holdings, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20130213
Source listing expiry
20261231

Source-listed ingredients

  • PIOGLITAZONE HYDROCHLORIDE — 15 mg/1
  • METFORMIN HYDROCHLORIDE — 850 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED in 1 BOTTLE (57237-218-60) · 57237-218-60
  • 180 TABLET, FILM COATED in 1 BOTTLE (57237-218-81) · 57237-218-81

Source and coverage

Open FDA National Drug Code directory

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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Pioglitazone Hydrochloride and Metformin Hydrochloride — United States | Molindra Medicines