United States · FDA National Drug Code directory

glyburide-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
23155-235_6a256976-cf1a-421b-86cb-452fddc75294
Product NDC
23155-235
Form
TABLET
Composition / generic term
glyburide-metformin hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240501
Source listing expiry
20271231

Source-listed ingredients

  • GLYBURIDE — 5 mg/1
  • METFORMIN HYDROCHLORIDE — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (23155-235-01) · 23155-235-01
  • 500 TABLET in 1 BOTTLE (23155-235-05) · 23155-235-05
  • 1000 TABLET in 1 BOTTLE (23155-235-10) · 23155-235-10

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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