United States · FDA National Drug Code directory

Glipizide

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
67046-0367_53e67073-8a11-c8b0-e063-6294a90a90cc
Product NDC
67046-0367
Form
TABLET
Composition / generic term
Glipizide
Labeler
Coupler LLC
Marketing category
ANDA
Marketing start / end (source format)
20260610
Source listing expiry
20271231

Source-listed ingredients

  • GLIPIZIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BLISTER PACK (67046-0367-3) · 67046-0367-3

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.

Browse United States records →