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
71610-680_737c6102-3cac-4ef5-812b-13e0298c7210
Product NDC
71610-680
Form
TABLET
Composition / generic term
Glipizide
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
19950831
Source listing expiry
20261231

Source-listed ingredients

  • GLIPIZIDE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 45 TABLET in 1 BOTTLE (71610-680-45) · 71610-680-45
  • 90 TABLET in 1 BOTTLE (71610-680-60) · 71610-680-60
  • 135 TABLET in 1 BOTTLE (71610-680-73) · 71610-680-73
  • 180 TABLET in 1 BOTTLE (71610-680-80) · 71610-680-80
  • 270 TABLET in 1 BOTTLE (71610-680-92) · 71610-680-92
  • 540 TABLET in 1 BOTTLE (71610-680-98) · 71610-680-98

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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